Nelson Textbook of Pediatrics, 2-Volume

Höfundur Robert M. Kliegman, Joseph W. St. Geme III

Útgefandi Elsevier Limited (UK)

Snið ePub

Print ISBN 9780323883054

Útgáfa 22

Útgáfuár 2025

17.890 kr.

Description

Efnisyfirlit

  • Cover image
  • Title page
  • Table of Contents
  • In Memory
  • Copyright
  • Dedication
  • Contributors
  • Preface
  • Volume 1
  • Part I. The Field of Pediatrics
  • Chapter 1. Overview of Pediatrics
  • Vital Statistics About Children’s Health Globally
  • The Changing Pediatric World
  • The New Normal: Pandemics
  • The New Morbidities
  • Chronic Illness and Children with Special Healthcare Needs
  • Systems of Care
  • Chapter 2. Child Health Disparities
  • Root Historical Causes of Structural Determinants of Health and Health Disparities
  • 2.1. Racism and Child Health
  • Chapter 3. Global Child Health
  • Global Burden and Trends in Child Health
  • The Social Determinants of Child Health and the COVID-19 Pandemic
  • Evidence-Based Interventions and Innovations to Address Child Health Inequities
  • Challenges in Global Health
  • Chapter 4. Quality and Value in Healthcare for Children
  • The Need for Improvement in Quality and Value
  • What are Quality and Value?
  • Frameworks for Quality Improvement
  • Measuring Quality
  • Analyzing Quality Data
  • Expanding Individual Quality Improvement Initiatives to Scale
  • Comparing and Reporting Quality
  • Implications of the U.S. Healthcare Reform for Quality
  • Chapter 5. Safety in Healthcare for Children
  • Error VS Harm
  • Safety Frameworks
  • Identifying and Analyzing Harm, Errors, and Latent Threats
  • Safety Culture
  • Reliability Science, Human Factors Engineering, and High-Reliability Organizations
  • Serious Harm Events and Healthcare-Associated Conditions
  • Safety Opportunities and Gaps
  • Emerging Areas of Safety Research and Improvement
  • Chapter 6. Ethics in Pediatric Care
  • Assent and Parental Permission
  • Treatment of Critically ill Children
  • Neonatal Ethics
  • Declaring Death and Organ Donation
  • Religious or Cultural Objections to Treatment
  • Pediatric Ethics Committees and Ethics Consultation
  • Newborn Screening
  • Genetics, Genomics, and Precision Medicine
  • Adolescent Healthcare
  • Research
  • Justice and Pediatric Ethics
  • Chapter 7. Complementary Therapies and Integrative Medicine
  • Dietary Supplements
  • Dietary Supplement Safety
  • Dietary Supplement Efficacy
  • Massage and Chiropractic
  • Mind-Body Therapies
  • Acupuncture
  • Cannabis
  • Internet Resources
  • Chapter 8. Pediatric Palliative Care
  • Goals of Care and Decision-Making
  • Advance Care Planning
  • Care Settings
  • Communication and Anticipatory Guidance
  • Chapter 9. Domestic and International Adoption
  • Domestic Adoption
  • Intercountry Adoption
  • Role of Pediatricians
  • Chapter 10. Foster and Kinship Care
  • Epidemiology
  • Legislation in the United States
  • Early Childhood Trauma Leads to Poor Health Outcomes
  • Health Issues
  • Healthcare for Children and Adolescents in Foster Care
  • Chapter 11. Medical Evaluation of the Foreign-Born Child
  • Commonly Encountered Infections
  • Immunizations
  • Chapter 12. Cultural Issues in Pediatric Care
  • What is Culture?
  • Culturally Informed Care
  • Chapter 13. Maximizing Children’s Health: Screening, Anticipatory Guidance, and Counseling
  • The Periodicity Schedule and Guidelines
  • Tasks of Well-Child Care
  • Infancy and Early Childhood
  • Middle Childhood and Adolescence
  • Office Intervention for Behavioral and Mental Health Issues
  • Evidence
  • Caring for the Child and Youth in the Context of the Family and Community
  • Chapter 14. Injury Control
  • Scope of the Problem
  • Principles of Injury Control
  • Risk Factors for Childhood Injuries
  • Mechanisms of Injury
  • Psychosocial Consequences of Injuries
  • Chapter 15. Impact of Violence Exposure on Children
  • Impacts of Violence
  • 15.1. Bullying, Cyberbullying, and School Violence
  • 15.2. Media Violence
  • 15.3. Effects of War on Children
  • Chapter 16. Child Trafficking for Sex and Labor
  • Clinical Presentation
  • Approach to the Patient at Risk for Trafficking
  • Examination and Diagnostic Testing
  • Referrals and Resources
  • Chapter 17. Abused and Neglected Children
  • Definitions
  • 17.1. Sexual Abuse
  • 17.2. Factitious Disorder Imposed on Another: Medical Child Abuse (Munchausen Syndrome by Proxy)
  • Chapter 18. Strategies for Health Behavior Change
  • Unified Theory of Behavior Change
  • Transtheoretical Model of Health Behavior Change
  • Common Factors Approach
  • Motivational Interviewing
  • Shared Decision-Making
  • Part II. Growth, Development, and Behavior
  • Chapter 19. Developmental and Behavioral Theories
  • BIOPSYCHOSOCIAL MODEL AND ECOBIODEVELOPMENTAL FRAMEWORK: MODELS OF DEVELOPMENT
  • Chapter 20. Positive Parenting and Support
  • THE IMPORTANCE OF PARENTING
  • THE ROLE OF THE FAMILY
  • PARENTING STYLES
  • CHILD TEMPERAMENT
  • CHILD BEHAVIORAL PROBLEMS
  • DEFINING POSITIVE PARENTING
  • PARENTING AS AN INTERVENTION
  • THE ROLE OF THE PEDIATRICIAN
  • DISCIPLINE/PUNISHMENT
  • Chapter 21. Assessment of Fetal Growth and Development
  • SOMATIC DEVELOPMENT
  • NEUROLOGIC DEVELOPMENT
  • BEHAVIORAL DEVELOPMENT
  • PSYCHOLOGIC CHANGES IN PARENTS
  • THREATS TO FETAL DEVELOPMENT
  • Chapter 22. The Newborn
  • PARENTAL ROLE IN PARENT–INFANT ATTACHMENT
  • THE INFANT’S ROLE IN PARENT–INFANT ATTACHMENT
  • IMPLICATIONS FOR THE PEDIATRICIAN
  • Chapter 23. The First Year
  • Age 0-2 Months
  • 23.1. Infant Crying and Colic
  • Chapter 24. The Second Year
  • Age 12–18 Months
  • Age 18–24 Months
  • Chapter 25. The Preschool Years
  • Structural Development of the Brain
  • Physical Development
  • Language, Cognition, and Play
  • Chapter 26. Middle Childhood
  • Physical Development
  • Cognitive Development
  • Social, Emotional, and Moral Development
  • Chapter 27. Assessment of Growth
  • Techniques to Measure Growth
  • Growth Curves
  • Other Growth Considerations
  • Chapter 28. Developmental and Behavioral Surveillance and Screening
  • Developmental and Behavioral Surveillance
  • Developmental and Behavioral Screening
  • Beyond Surveillance and Screening
  • Chapter 29. Child Care
  • Quality, Provision, Regulation, and Access
  • Screening and Support for Child Development and Health
  • Role of Pediatric Providers
  • Chapter 30. Loss, Separation, and Bereavement
  • Separation and Loss
  • Divorce
  • Move/Family Relocation
  • Separation Because of Hospitalization
  • Military Families
  • Parental/Sibling Death
  • Grief and Bereavement
  • Developmental Perspective
  • Role of the Pediatric Healthcare Provider in Grief
  • Treatment
  • Spiritual Issues
  • Chapter 31. Sleep Medicine
  • Basics of Sleep and Chronobiology
  • Developmental Changes in Sleep
  • Common Sleep Disorders
  • Sleep Health Supervision
  • Evaluation of Pediatric Sleep Problems
  • Part III. Behavioral and Psychiatric Disorders
  • Chapter 32. Psychosocial Assessment and Psychiatric Diagnostic Evaluation
  • AIMS OF PSYCHOSOCIAL ASSESSMENT IN THE PEDIATRIC SETTING
  • PRESENTING PROBLEMS
  • GENERAL PRINCIPLES OF THE PSYCHOSOCIAL INTERVIEW
  • DIAGNOSIS
  • PSYCHIATRIC DIAGNOSTIC EVALUATION
  • SPECIAL CONSIDERATIONS IN THE DIAGNOSTIC EVALUATION OF INFANTS AND YOUNG CHILDREN
  • Chapter 33. Psychopharmacology
  • Stimulants and Other ADHD Medications
  • Antidepressants
  • Antipsychotics
  • Mood Stabilizers
  • Medication Use in Physical Illness
  • Chapter 34. Psychotherapy
  • Psychotherapy
  • Chapter 35. Somatic Symptom and Related Disorders
  • SOMATIZATION
  • RISK FACTORS FOR SOMATIZATION
  • ASSESSMENT
  • MANAGEMENT
  • Chapter 36. Rumination and Pica
  • 36.1. Rumination Disorder
  • 36.2. Pica
  • Chapter 37. Motor Disorders and Habits
  • 37.1. Tic Disorders
  • 37.2. Stereotypic Movement Disorder
  • Chapter 38. Anxiety Disorders, Obsessive-Compulsive Disorder, and Posttraumatic Stress Disorder
  • ASSESSMENT
  • DIFFERENTIAL DIAGNOSIS AND COMORBIDITIES
  • Treatment of Anxiety
  • Obsessive-Compulsive Disorder and Pediatric Acute-Onset Neuropsychiatric Syndrome
  • SPECIFIC PHOBIAS
  • Chapter 39. Mood Disorders
  • 39.1. Depressive Disorders
  • 39.2. Bipolar Disorders
  • Chapter 40. Suicide and Attempted Suicide
  • Epidemiology
  • Risk Factors
  • Assessment and Intervention
  • Prevention
  • Screening and Early Treatment
  • School Resources
  • Chapter 41. Eating Disorders
  • DEFINITIONS
  • EPIDEMIOLOGY
  • PATHOLOGY AND PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIFFERENTIAL DIAGNOSIS
  • LABORATORY FINDINGS
  • COMPLICATIONS
  • TREATMENT
  • PROGNOSIS
  • PREVENTION
  • Chapter 42. Disruptive, Impulse-Control, and Conduct Disorders
  • DESCRIPTION
  • EPIDEMIOLOGY
  • CLINICAL COURSE
  • DIFFERENTIAL DIAGNOSIS
  • COMORBIDITY
  • SEQUELAE
  • ETIOLOGY AND RISK FACTORS
  • PREVENTION
  • SCREENING/CASE FINDING
  • EARLY INTERVENTION
  • TREATMENT
  • LEVEL OF CARE
  • Chapter 43. Tantrums and Breath-Holding Spells
  • Chapter 44. Lying, Stealing, and Truancy
  • STEALING
  • TRUANCY
  • Chapter 45. Aggression
  • Chapter 46. Self-Injurious Behavior
  • Chapter 47. Childhood Psychoses
  • 47.1. Schizophrenia Spectrum Disorders
  • 47.2. Non-Schizophrenia Spectrum Psychotic Disorders
  • 47.3. Catatonia in Children and Adolescents
  • 47.4. Hallucinations of Childhood
  • Chapter 48. Delirium
  • DIAGNOSIS
  • EPIDEMIOLOGY
  • ETIOLOGY
  • ASSESSMENT
  • RATING SCALES
  • MEDICAL EVALUATION
  • DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • Part IV. Learning and Developmental Disorders
  • Chapter 49. Neurodevelopmental and Executive Function and Dysfunction
  • TERMINOLOGY AND EPIDEMIOLOGY
  • ETIOLOGY AND PATHOGENESIS
  • CORE NEURODEVELOPMENTAL FUNCTIONS
  • CLINICAL MANIFESTATIONS
  • ASSESSMENT AND DIAGNOSIS
  • TREATMENT
  • COUNSELING AND PARENT TRAINING PROGRAMS
  • Chapter 50. Attention-Deficit/Hyperactivity Disorder
  • EPIDEMIOLOGY
  • ETIOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • SECONDARY PREVENTION
  • Chapter 51. Dyslexia
  • DEFINITION
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • IS FAMILY HISTORY HELPFUL IN DIAGNOSING DYSLEXIA?
  • MANAGEMENT
  • Prognosis
  • Chapter 52. Math and Writing Disabilities
  • 52.1. Math Disabilities
  • 52.2. Writing Disabilities
  • Chapter 53. Language Development and Communication Disorders
  • TYPICAL DEVELOPMENT
  • 53.1. Childhood-Onset Fluency Disorder
  • Chapter 54. Augmentative and Alternative Communication
  • DEFINITIONS
  • Chapter 55. Outcomes Among Infants and Children Who Are Deaf/Hard of Hearing
  • DEAF CULTURE
  • EARLY DETECTION AND LANGUAGE DEVELOPMENT
  • INTERVENTIONS
  • LANGUAGE LEARNING
  • ACADEMIC CONSIDERATIONS
  • PSYCHOSOCIAL WELL-BEING
  • DEAF PLUS
  • FAMILY JOURNEY
  • Acknowledgments
  • Chapter 56. Developmental Delay and Intellectual Disability
  • DEFINITION
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOLOGY AND PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • ETIOLOGIC EVALUATION
  • DIFFERENTIAL DIAGNOSIS
  • DIAGNOSTIC PSYCHOLOGIC TESTING
  • COMPLICATIONS AND ASSOCIATED CONDITIONS
  • PREVENTION
  • TREATMENT
  • PRIMARY CARE, SUPPORTIVE CARE, AND MANAGEMENT
  • OUTCOMES
  • Chapter 57. Down Syndrome and Other Abnormalities of Chromosome Number
  • PRINCIPLES OF CARING FOR CHILDREN WITH COMPLEX GENETIC DISORDERS
  • CLINICAL CHARACTERISTICS
  • DEVELOPMENTAL AND BEHAVIORAL CHARACTERISTICS
  • Chapter 58. Autism Spectrum Disorder
  • DEFINITION
  • DIAGNOSTIC CRITERIA AND SYMPTOMS
  • EPIDEMIOLOGY
  • ETIOLOGY
  • DIFFERENTIAL DIAGNOSIS
  • CO-OCCURRING CONDITIONS
  • SCREENING
  • ASSESSMENT
  • TREATMENT AND MANAGEMENT
  • OUTCOME
  • Chapter 59. Fragile X Syndromes
  • EVALUATION AND DIAGNOSIS
  • MANAGEMENT OF FRAGILE X SYNDROME
  • Part V. Nutrition
  • Chapter 60. Nutritional Requirements
  • DIETARY REFERENCE INTAKES
  • ENERGY
  • FAT
  • PROTEIN
  • CARBOHYDRATES
  • FIBER
  • MICRONUTRIENTS
  • WATER
  • MEASURING NUTRITIONAL ADEQUACY
  • Chapter 61. Feeding Healthy Infants, Children, and Adolescents
  • FEEDING DURING THE FIRST YEAR OF LIFE
  • COW’S MILK PROTEIN–BASED FORMULAS
  • SOY PROTEIN–BASED FORMULAS
  • PROTEIN HYDROLYSATE FORMULAS
  • AMINO ACID FORMULAS
  • OTHER FLUIDS IN INFANTS AND TODDLERS
  • COMPLEMENTARY FEEDING
  • TRANSITION TO MILK
  • RESPONSIVE FEEDING
  • FEEDING TODDLERS AND PRESCHOOL-AGED CHILDREN
  • FEEDING SCHOOL-AGED CHILDREN AND ADOLESCENTS
  • NUTRITION ISSUES OF IMPORTANCE ACROSS PEDIATRIC AGES
  • Chapter 62. Nutrition, Food Security, and Health
  • MALNUTRITION AS THE INTERSECTION OF FOOD INSECURITY AND HEALTH INSECURITY
  • FOOD SECURITY
  • UNDERNUTRITION
  • SEVERE ACUTE MALNUTRITION
  • Chapter 63. Refeeding Syndrome
  • Chapter 64. Malnutrition in High-Resource Settings
  • CLINICAL MANIFESTATIONS
  • ETIOLOGY AND DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • Chapter 65. Overweight and Obesity
  • EPIDEMIOLOGY
  • BODY MASS INDEX
  • ETIOLOGY
  • COMORBIDITIES
  • IDENTIFICATION
  • EVALUATION
  • INTERVENTION
  • PREVENTION
  • Chapter 66. Vitamin A Deficiencies and Excess
  • OVERVIEW OF VITAMIN A
  • METABOLISM OF VITAMIN A
  • FUNCTIONS OF VITAMIN A AND MECHANISMS OF ACTION
  • VITAMIN A DEFICIENCY
  • HYPERVITAMINOSIS A
  • Chapter 67. Vitamin B Complex Deficiencies and Excess
  • 67.1. Thiamine (Vitamin B1)
  • 67.2. Riboflavin (Vitamin B2)
  • 67.3. Niacin (Vitamin B3)
  • 67.4. Vitamin B6 (Pyridoxine)
  • 67.5. Biotin
  • 67.6. Folate
  • 67.7. Vitamin B12 (Cobalamin)
  • Chapter 68. Vitamin C (Ascorbic Acid) Deficiency and Excess
  • DIETARY NEEDS AND SOURCES OF VITAMIN C
  • VITAMIN C DEFICIENCY
  • VITAMIN C TOXICITY
  • Chapter 69. Vitamin D Deficiency (Rickets) and Excess
  • RICKETS
  • VITAMIN D DISORDERS
  • CALCIUM DEFICIENCY
  • PHOSPHORUS DEFICIENCY
  • RICKETS OF PREMATURITY
  • DISTAL RENAL TUBULAR ACIDOSIS
  • HYPERVITAMINOSIS D
  • Chapter 70. Vitamin E Deficiency
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS
  • DIAGNOSIS AND DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • PREVENTION
  • Chapter 71. Vitamin K Deficiency
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS AND DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • PREVENTION
  • Chapter 72. Micronutrient Mineral Deficiencies
  • Part VI. Fluid and Electrolyte Disorders
  • Chapter 73. Electrolyte and Acid-Base Disorders
  • 73.1. Composition of Body Fluids
  • 73.2. Regulation of Osmolality and Volume
  • 73.3. Sodium
  • 73.4. Potassium
  • 73.5. Magnesium
  • 73.6. Phosphorus
  • 73.7. Acid-Base Balance
  • Chapter 74. Maintenance and Replacement Therapy
  • MAINTENANCE THERAPY
  • MAINTENANCE WATER
  • INTRAVENOUS SOLUTIONS
  • GLUCOSE
  • SELECTION OF MAINTENANCE FLUIDS
  • VARIATIONS IN MAINTENANCE WATER AND ELECTROLYTES
  • REPLACEMENT FLUIDS
  • Chapter 75. Deficit Therapy
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS
  • CALCULATION OF THE FLUID DEFICIT
  • APPROACH TO SEVERE DEHYDRATION
  • MONITORING AND ADJUSTING THERAPY
  • HYPONATREMIC DEHYDRATION
  • HYPERNATREMIC DEHYDRATION
  • Chapter 76. Fluid and Electrolyte Treatment of Specific Disorders
  • ACUTE DIARRHEA
  • PYLORIC STENOSIS
  • PERIOPERATIVE FLUIDS
  • Part VII. Emergency Medicine, Critical Care, and Anesthesia
  • Chapter 77. Emergency Medical Services for Children
  • PRIMARY CARE PHYSICIAN AND OFFICE PREPAREDNESS
  • 77.1. Interfacility Transport of the Seriously Ill or Injured Pediatric Patient
  • 77.2. Risk Adjustment and Outcomes Measurement of Pediatric Emergency Medical Services
  • 77.3. Principles Applicable to the Developing World
  • Chapter 78. Triage of the Acutely Ill Child
  • ASSESSMENT OF VITAL SIGNS
  • HISTORY
  • PHYSICAL EXAMINATION
  • MANAGEMENT
  • DISPOSITION
  • Chapter 79. Pediatric Cardiorespiratory Emergencies and Resuscitation
  • ASSESSMENT AND EVALUATION OF CHILDREN WITH CARDIORESPIRATORY EMERGENCIES
  • RECOGNITION AND TREATMENT OF RESPIRATORY DISTRESS AND FAILURE
  • RECOGNITION AND MANAGEMENT OF SHOCK
  • RECOGNITION AND TREATMENT OF ARRHYTHMIAS
  • CARDIAC ARREST AND CARDIOPULMONARY RESUSCITATION
  • PROCEDURES
  • NONVASCULAR EMERGENCY PROCEDURES
  • Chapter 80. Acute Care of Multiple Trauma
  • EPIDEMIOLOGY
  • REGIONALIZATION AND TRAUMA TEAMS
  • ATLS: SYSTEMATIC EVALUATION OF THEINJURED PATIENT
  • PRIMARY SURVEY
  • SECONDARY SURVEY
  • DISPOSITION
  • PSYCHOLOGIC AND SOCIAL SUPPORT
  • Chapter 81. Spinal Cord Injuries in Children
  • CLINICAL MANIFESTATIONS
  • CLEARING THE CERVICAL SPINE IN CHILDREN
  • TREATMENT
  • PREVENTION
  • Chapter 82. Neurologic Emergencies and Stabilization
  • NEUROCRITICAL CARE PRINCIPLES
  • TRAUMATIC BRAIN INJURY
  • Chapter 83. Brain Death: Death by Neurologic Criteria
  • EPIDEMIOLOGY
  • CLINICAL EVALUATION AND DIAGNOSIS
  • OBSERVATION PERIODS
  • ANCILLARY STUDIES
  • DOCUMENTATION
  • AFTER DECLARATION OF BRAIN DEATH
  • OBJECTIONS TO THE CONCEPT OF BRAIN DEATH
  • Chapter 84. Syncope
  • MECHANISMS
  • 84.1. Postural Tachycardia Syndrome
  • Chapter 85. Shock
  • EPIDEMIOLOGY
  • TYPES OF SHOCK
  • PATHOPHYSIOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • LABORATORY FINDINGS
  • TREATMENT
  • PROGNOSIS
  • Chapter 86. Acute Care of Respiratory Distress and Failure
  • RESPIRATORY DISTRESS
  • 86.1. Mechanical Ventilation
  • Chapter 87. Altitude-Associated Illness in Children
  • ETIOLOGY
  • ACUTE MOUNTAIN SICKNESS
  • HIGH-ALTITUDE CEREBRAL EDEMA
  • HIGH-ALTITUDE PULMONARY EDEMA
  • SPECIAL CONSIDERATIONS
  • Acknowledgments
  • Chapter 88. Drowning and Submersion Injury
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOPHYSIOLOGY
  • MANAGEMENT
  • PROGNOSIS
  • PREVENTION
  • Chapter 89. Burn Injuries
  • EPIDEMIOLOGY
  • 89.1. Lightning Burns
  • Chapter 90. Cold Injuries
  • MECHANISMS OF HEAT TRANSFER
  • 90.1. Cold-Induced Autoinflammatory and Other Genetic Disorders
  • Chapter 91. Anesthesia and Perioperative Care
  • PREANESTHETIC EVALUATION
  • 91.1. Anesthetic Neurotoxicity
  • Chapter 92. Procedural Sedation
  • Chapter 93. Pediatric Pain Management
  • DEFINITION AND CATEGORIES OF PAIN
  • ASSESSMENT AND MEASUREMENT OF PAIN IN CHILDREN
  • CONCEPTUAL FRAMEWORK FOR TREATMENT OF PEDIATRIC PAIN
  • UNCONVENTIONAL MEDICATIONS IN PEDIATRIC PAIN
  • NONPHARMACOLOGIC TREATMENT OF PAIN
  • INVASIVE INTERVENTIONS FOR TREATING PAIN
  • INTRATHECAL ANALGESIA
  • NERVE ABLATION AND DESTRUCTION
  • CONSIDERATIONS FOR SPECIAL PEDIATRIC POPULATIONS
  • CHRONIC AND RECURRENT PAIN SYNDROMES
  • MANAGING COMPLEX CHRONIC PAIN PROBLEMS
  • Chapter 94. Poisoning
  • PREVENTION
  • APPROACH TO THE POISONED PATIENT
  • PRINCIPLES OF MANAGEMENT
  • SELECT COMPOUNDS IN PEDIATRIC POISONING
  • Part VIII. Human Genetics
  • Chapter 95. Genetics in Pediatric Medicine
  • THE BURDEN OF GENETIC DISORDERS IN CHILDHOOD
  • THE CHANGING PARADIGM OF GENETICS IN MEDICINE
  • DIRECT-TO-CONSUMER GENETIC TESTING
  • ETHICS ISSUES
  • Chapter 96. Principles of Human Genetics
  • THE HUMAN GENOME
  • FUNDAMENTALS OF MOLECULAR GENETICS
  • GENETIC VARIATION
  • GENOTYPE-PHENOTYPE CORRELATIONS IN GENETIC DISEASE
  • HUMAN GENOME PROJECT
  • Chapter 97. Patterns of Genetic Transmission
  • FAMILY HISTORY AND PEDIGREE NOTATION
  • MENDELIAN INHERITANCE
  • Y-LINKED INHERITANCE
  • INHERITANCE ASSOCIATED WITH PSEUDOAUTOSOMAL REGIONS
  • DIGENIC INHERITANCE
  • PSEUDOGENETIC INHERITANCE AND FAMILIAL CLUSTERING
  • NONTRADITIONAL INHERITANCE
  • MULTIFACTORIAL AND POLYGENIC INHERITANCE
  • Chapter 98. Integration of Genetics into Pediatric Practice
  • DIAGNOSTIC TESTING
  • PHARMACOGENETICS
  • 98.1. Genetic Counseling
  • 98.2. Principles of Management and Treatment of Genetic Disorders
  • Chapter 99. Chromosome Disorders
  • 99.1. Methods of Chromosome Analysis
  • 99.2. Abnormalities of Chromosome Number
  • 99.3. Abnormalities of Chromosome Structure
  • 99.4. Sex Chromosome Aneuploidy
  • 99.5. Mosaicism
  • 99.6. Chromosome Instability Syndromes
  • 99.7. Uniparental Disomy and Imprinting
  • Chapter 100. Dysmorphology, Phenotyping, and Sequences
  • CLASSIFICATION OF BIRTH DEFECTS
  • MOLECULAR MECHANISMS OF MALFORMATIONS
  • APPROACH TO THE CHILD WITH FACIAL ANOMALIES
  • Chapter 101. Signaling Pathway Disorders
  • 101.1. RAS/MAPK Pathway
  • 101.2. Sonic Hedgehog Pathway
  • 101.3. Ciliopathies
  • 101.4. Craniosynostoses
  • Chapter 102. Chromatin Regulatory Disorders
  • KABUKI SYNDROME
  • RUBINSTEIN-TAYBI SYNDROME
  • CORNELIA DE LANGE SYNDROME
  • COFFIN-SIRIS SYNDROME
  • OTHER CHROMATIN DISORDERS
  • Chapter 103. Genetics of Common Disorders
  • 103.1. Major Genetic Approaches to the Study of Common Pediatric Disorders
  • Part IX. Metabolic Disorders
  • Chapter 104. An Approach to Inborn Errors of Metabolism
  • NEWBORN SCREENING
  • CLINICAL MANIFESTATIONS OF GENETIC METABOLIC DISEASES
  • TREATMENT
  • Chapter 105. Defects in Metabolism of Amino Acids
  • 105.1. Phenylalanine
  • 105.2. Tyrosine
  • 105.3. Methionine
  • 105.4. Cysteine and Cystine
  • 105.5. Tryptophan
  • 105.6. Isoleucine, Leucine, Valine, and Related Organic Acidemias
  • 105.7. Glycine
  • 105.8. Serine Deficiency Disorders (Serine Biosynthesis and Transport Defects)
  • 105.9. Proline
  • 105.10. Glutamic Acid
  • 105.11. Disorders of Neurotransmitter Metabolism
  • 105.12. Urea Cycle and Hyperammonemia (Arginine, Citrulline, Ornithine)
  • 105.13. Histidine
  • 105.14. Lysine
  • 105.15. N-Acetylaspartic Acid (Canavan Disease)
  • Chapter 106. Defects in Metabolism of Lipids
  • 106.1. Disorders of Mitochondrial Fatty Acid β-Oxidation
  • 106.2. Disorders of Very Long Chain Fatty Acids and Other Peroxisomal Functions
  • 106.3. Disorders of Lipoprotein Metabolism and Transport
  • 106.4. Lipidoses (Lysosomal Storage Disorders)
  • 106.5. Mucolipidoses
  • Chapter 107. Defects in Metabolism of Carbohydrates
  • 107.1. Glycogen Storage Diseases
  • 107.2. Defects in Galactose Metabolism
  • 107.3. Defects in Fructose Metabolism
  • 107.4. Defects in Intermediary Carbohydrate Metabolism Associated with Lactic Acidosis
  • 107.5. Defects in Pentose Metabolism
  • 107.6. Disorders of Glycoprotein Degradation and Structure
  • 107.7. Congenital Disorders of Glycosylation
  • Chapter 108. Mitochondrial Disease Diagnosis
  • WHEN TO SUSPECT MITOCHONDRIAL DISEASE
  • MITOCHONDRIAL DISEASE INHERITANCE
  • DIAGNOSTIC TESTING FOR MITOCHONDRIAL DISEASE
  • TREATMENT PRINCIPLES FOR MITOCHONDRIAL DISEASE
  • Chapter 109. Mucopolysaccharidoses
  • CLINICAL ENTITIES
  • DIAGNOSIS AND DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • Chapter 110. Disorders of Purine and Pyrimidine Metabolism
  • PURINES
  • PYRIMIDINES
  • DISORDERS OF PURINE METABOLISM
  • THE HEREDITARY XANTHINURIAS
  • HPRT1-ASSOCIATED DISORDERS
  • APRT-ASSOCIATED DISORDERS
  • DISORDERS ASSOCIATED WITH AMP-DEAMINASE
  • ADSL-ASSOCIATED DISORDERS
  • OTHER INHERITED PURINE DISORDERS
  • DISORDERS OF PYRIMIDINE METABOLISM
  • DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY
  • DISORDERS ASSOCIATED WITH THYMIDINE KINASE
  • COMBINED DISORDERS OF BOTH PURINES AND PYRIMIDINES
  • DISORDERS ASSOCIATED WITH RIBONUCLEOTIDE REDUCTASE
  • Chapter 111. Hutchinson-Gilford Progeria Syndrome (Progeria)
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS
  • MOLECULAR PATHOGENESIS
  • DIAGNOSIS AND DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • PATIENT RESOURCES
  • Chapter 112. The Porphyrias
  • THE HEME BIOSYNTHETIC PATHWAY
  • CLASSIFICATION AND DIAGNOSIS OF PORPHYRIAS
  • δ-AMINOLEVULINIC ACID DEHYDRATASE–DEFICIENT PORPHYRIA
  • ACUTE INTERMITTENT PORPHYRIA
  • CONGENITAL ERYTHROPOIETIC PORPHYRIA
  • PORPHYRIA CUTANEA TARDA
  • HEPATOERYTHROPOIETIC PORPHYRIA
  • HEREDITARY COPROPORPHYRIA
  • VARIEGATE PORPHYRIA
  • ERYTHROPOIETIC PROTOPORPHYRIA AND X-LINKED PROTOPORPHYRIA
  • DUAL PORPHYRIA
  • PORPHYRIA RESULTING FROM TUMORS
  • Chapter 113. Hypoglycemia
  • DEFINITION
  • SIGNIFICANCE AND SEQUELAE
  • PHYSIOLOGIC MECHANISMS OF GLUCOSE HOMEOSTASIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • MANAGEMENT
  • DISORDERS OF HYPOGLYCEMIA
  • KETOTIC HYPOGLYCEMIC DISORDERS
  • OTHER CAUSES OF HYPOGLYCEMIA
  • Part X. The Fetus and the Neonatal Infant
  • Chapter 114. Overview of Morbidity and Mortality
  • INFANT MORTALITY
  • 114.1. Race, Class, and Birth Outcomes
  • Chapter 115. The Newborn Infant
  • 115.1. Focused Peripartum History
  • 115.2. Physical Examination of the Newborn Infant
  • 115.3. Routine Newborn Care
  • 115.4. Male Circumcision
  • 115.5. Parent–Infant Bonding
  • Chapter 116. High-Risk Pregnancies
  • PRENATAL CARE
  • HIGH-RISK PREGNANCY IDENTIFIED BY ULTRASOUND
  • LABOR AND DELIVERY
  • Chapter 117. The Fetus
  • 117.1. Fetal Growth and Maturity
  • 117.2. Fetal Distress
  • 117.3. Maternal Disease and the Fetus
  • 117.4. Medications and Teratogenic Exposures
  • 117.5. Radiation
  • 117.6. Intrauterine Diagnosis of Fetal Disease
  • 117.7. Treatment and Prevention of Fetal Disease
  • Chapter 118. Fetal Intervention and Surgery
  • FETAL THERAPY ETHICS
  • OBSTRUCTIVE UROPATHY
  • NONOBSTRUCTIVE RENAL DISEASE
  • CONGENITAL DIAPHRAGMATIC HERNIA
  • CONGENITAL PULMONARY AIRWAY MALFORMATION
  • CONGENITAL HIGH AIRWAY OBSTRUCTION SYNDROME
  • SACROCOCCYGEAL TERATOMA
  • MYELOMENINGOCELE
  • TWIN-TO-TWIN TRANSFUSION SYNDROME
  • OTHER INDICATIONS
  • FETAL CENTERS
  • Chapter 119. The High-Risk Infant
  • 119.1. Multiple-Gestation Pregnancies
  • 119.2. Extremely and Very Preterm Infants
  • 119.3. Moderate and Late Preterm Infants
  • 119.4. Term and Postterm Infants
  • 119.5. Follow-Up of High-Risk Infants After Discharge
  • Chapter 120. Transport of the Critically Ill Newborn
  • REGIONALIZED CARE OF NEWBORNS
  • LEVELS OF NEONATAL CARE
  • TRANSPORT OF THE CRITICALLY ILL NEONATE
  • Chapter 121. Clinical Manifestations of Diseases in the Newborn Period
  • ABNORMAL MOVEMENTS
  • 121.1. Hyperthermia
  • 121.2. Hypothermia and Cold Stress
  • 121.3. Edema
  • 121.4. Hypocalcemia
  • 121.5. Hypermagnesemia
  • Chapter 122. Nervous System Disorders
  • 122.1. The Cranium
  • 122.2. Neonatal Traumatic Head Injuries
  • 122.3. Intracranial-Intraventricular Hemorrhage and Periventricular Leukomalacia
  • 122.4. Hypoxic-Ischemic Encephalopathy
  • 122.5. Spine and Spinal Cord
  • 122.6. Peripheral Nerve Injuries
  • Chapter 123. Neonatal Resuscitation and Delivery Room Emergencies
  • NEONATAL RESUSCITATION
  • RESUSCITATION OF THE PRETERM INFANT
  • SPECIAL CIRCUMSTANCES IN THE DELIVERY ROOM
  • INJURY DURING DELIVERY
  • ONGOING CARE AFTER RESUSCITATION
  • Chapter 124. Transition to Newborn Pulmonary Respiration
  • CLEARANCE OF FETAL LUNG FLUID
  • ESTABLISHMENT OF A FUNCTIONAL RESIDUAL CAPACITY
  • INCREASED PULMONARY BLOOD FLOW
  • BREATHING PATTERNS IN NEWBORNS
  • DISORDERED TRANSITION TO PULMONARY RESPIRATION
  • Chapter 125. Apnea
  • OBSTRUCTIVE APNEA
  • CENTRAL APNEA
  • APNEA OF PREMATURITY
  • TREATMENT
  • PROGNOSIS
  • Chapter 126. Respiratory Distress Syndrome (Hyaline Membrane Disease)
  • INCIDENCE
  • 126.1. Patent Ductus Arteriosus
  • Chapter 127. Bronchopulmonary Dysplasia
  • INCIDENCE
  • ETIOLOGY AND PATHOPHYSIOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • PREVENTION
  • TREATMENT
  • PROGNOSIS
  • Chapter 128. Transient Tachypnea of the Newborn
  • INCIDENCE
  • ETIOLOGY AND PATHOPHYSIOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • PREVENTION
  • TREATMENT
  • Chapter 129. Aspiration of Foreign Material (Meconium Aspiration Syndrome, Aspiration Pneumonia)
  • INTRAPARTUM ASPIRATION
  • POSTPARTUM ASPIRATION
  • Chapter 130. Persistent Pulmonary Hypertension of the Newborn (Persistent Fetal Circulation)
  • PATHOPHYSIOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • Chapter 131. Diaphragmatic Hernia
  • CONGENITAL DIAPHRAGMATIC HERNIA (BOCHDALEK)
  • 131.1. Foramen of Morgagni Hernia
  • 131.2. Paraesophageal Hernia
  • 131.3. Eventration
  • Chapter 132. Pulmonary Air Leaks: Pneumothorax, Pneumomediastinum, Pulmonary Interstitial Emphysema, Pneumopericardium
  • ETIOLOGY AND PATHOPHYSIOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • PREVENTION
  • TREATMENT
  • Chapter 133. Pulmonary Hemorrhage
  • Chapter 134. Digestive System Disorders
  • Chapter 135. Meconium Ileus, Peritonitis, Intestinal Obstruction, and Gastroschisis
  • MECONIUM PLUGS
  • MECONIUM ILEUS
  • MECONIUM PERITONITIS
  • GASTROSCHISIS
  • Chapter 136. Necrotizing Enterocolitis
  • DEFINITION
  • EPIDEMIOLOGY
  • PATHOLOGY AND PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • PREVENTION
  • Chapter 137. Jaundice and Hyperbilirubinemia in the Newborn
  • ETIOLOGY
  • 137.1. Kernicterus and Therapy of Hyperbilirubinemia
  • Chapter 138. Blood Disorders
  • NORMAL ERYTHROPOIESIS AND HEMOGLOBIN FUNCTIONS
  • NORMAL RED BLOOD CELL INDICES IN NEONATES AND INFANTS
  • NEUTROPENIA
  • Chapter 139. Anemia in the Newborn Infant
  • THE PHYSIOLOGIC NADIR DURING INFANCY
  • ANEMIA CLASSIFICATIONS AND KEY DIAGNOSTIC MODALITIES
  • HEMOGLOBINOPATHIES
  • ANEMIA MANAGEMENT PRINCIPALS
  • Chapter 140. Hemolytic Disease of the Fetus and Newborn
  • HDFN CAUSED BY Rh INCOMPATIBILITY
  • HDFN CAUSED BY ABO INCOMPATIBILITY
  • OTHER ETIOLOGIES OF HDFN
  • Chapter 141. Neonatal Polycythemia
  • Chapter 142. Hemorrhage in the Newborn Infant
  • HEMORRHAGIC DISEASE OF THE NEWBORN
  • DISSEMINATED INTRAVASCULAR COAGULOPATHY
  • Chapter 143. Nonimmune Hydrops
  • INCIDENCE AND ETIOLOGY
  • PRENATAL DIAGNOSIS AND TREATMENT
  • POSTNATAL DIAGNOSIS AND TREATMENT
  • OUTCOMES
  • Chapter 144. The Umbilicus
  • UMBILICAL HEMORRHAGE
  • UMBILICAL GRANULOMA
  • UMBILICAL INFECTIONS
  • UMBILICAL HERNIA
  • CONGENITAL OMPHALOCELE
  • UMBILICAL TUMORS
  • Chapter 145. Neonatal Abstinence Syndrome
  • TREATMENT AND SETTING
  • Chapter 146. Fetal Alcohol Spectrum Disorder
  • EPIDEMIOLOGY
  • PREVALENCE
  • DIAGNOSTIC SYSTEMS
  • DIAGNOSTIC CRITERIA
  • DIFFERENTIAL DIAGNOSIS
  • OUTCOMES
  • INTERVENTIONS AND TREATMENTS
  • THE PEDIATRICIAN/PRIMARY CARE PROVIDER’S ROLE
  • Chapter 147. Infants of Diabetic Mothers
  • PATHOPHYSIOLOGY
  • CLINICAL MANIFESTATIONS
  • TREATMENT
  • PROGNOSIS
  • Chapter 148. Epidemiology of Infections
  • INCIDENCE
  • MICROBIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS
  • GENERAL APPROACH TO MANAGEMENT
  • PREVENTION
  • Chapter 149. Congenital and Perinatal Infections
  • 149.1. Congenital Infections
  • 149.2. Perinatal Infections
  • Part XI. Adolescent Medicine
  • Chapter 150. Adolescent Physical and Social Development
  • PHYSICAL DEVELOPMENT
  • NEUROLOGIC, COGNITIVE, AND MORAL DEVELOPMENT
  • PSYCHOSOCIAL DEVELOPMENT
  • IMPLICATIONS FOR PROVIDERS, PARENTS, AND POLICYMAKERS
  • Chapter 151. Delivery of Healthcare to Adolescents
  • Introduction
  • 151.1. Legal Issues
  • 151.2. Screening Procedures
  • Chapter 152. Transitioning to Adult Care
  • Chapter 153. Gender Identity and Transgender Care
  • TERMINOLOGY
  • EPIDEMIOLOGY
  • MENTAL HEALTH CONSIDERATIONS
  • PUBERTY BLOCKERS
  • GENDER-AFFIRMING SEX HORMONE THERAPY
  • THERAPY FOR NONBINARY YOUTH
  • Chapter 154. Gay, Lesbian, and Bisexual Adolescents
  • PREVALENCE OF HOMOSEXUALITY AND BISEXUALITY IN YOUTH
  • DEVELOPMENT OF SEXUAL ORIENTATION IN CHILDHOOD AND ADOLESCENCE
  • STIGMA, RISK, AND RESILIENCE
  • HEALTH
  • RECOMMENDATIONS FOR CARE
  • Chapter 155. The Epidemiology of Adolescent Health Problems
  • ACCESS TO HEALTHCARE
  • Chapter 156. Violent Behavior
  • EPIDEMIOLOGY
  • ETIOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PREVENTION
  • Chapter 157. Substance Use Disorder
  • ETIOLOGY
  • 157.1. Alcohol
  • 157.2. Tobacco, E-Cigarettes, and Other Tobacco Products
  • 157.3. Marijuana
  • 157.4. Inhalants
  • 157.5. EVALI
  • 157.6. Hallucinogens
  • 157.7. Cocaine
  • 157.8. Amphetamines
  • 157.9. Stimulant Use and Diversion
  • 157.10. Opiates/Opioids
  • 157.11. Synthetic Cannabinoids
  • Chapter 158. The Breast
  • FEMALE DISORDERS
  • MALE DISORDERS
  • Chapter 159. Menstruation-Related Disorders
  • NORMAL MENSTRUATION
  • 159.1. Amenorrhea
  • 159.2. Abnormal Uterine Bleeding
  • 159.3. Dysmenorrhea
  • 159.4. Premenstrual Syndrome and Premenstrual Dysphoric Disorder
  • Chapter 160. Contraception
  • CONTRACEPTIVE EFFECTIVENESS
  • 160.1. Contraceptive Use
  • 160.2. Contraceptive Counseling
  • 160.3. Long-Acting Reversible Contraception
  • 160.4. Other Progestin-Only Methods
  • 160.5. Combined Hormonal Contraceptives
  • 160.6. Emergency Contraception
  • 160.7. Condoms
  • 160.8. Other Barrier Methods
  • 160.9. Other Contraceptive Methods
  • Chapter 161. Adolescent Pregnancy
  • EPIDEMIOLOGY
  • 161.1. Abortion
  • Chapter 162. Adolescent Sexual Assault
  • EPIDEMIOLOGY
  • TERMINOLOGY
  • TYPES OF SEXUAL VIOLENCE
  • CLINICAL MANIFESTATIONS
  • INTERVIEW AND PHYSICAL EXAMINATION
  • LABORATORY DATA
  • TREATMENT
  • FOLLOW-UP
  • PREVENTION
  • Chapter 163. Sexually Transmitted Infections
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • SCREENING
  • COMMON INFECTIONS AND CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PREVENTION
  • Immunology
  • Section 1. Evaluation of the Immune System
  • Chapter 164. Orientation to the Consideration of Inborn Errors of Immunity
  • INFECTION RED FLAGS
  • SCHEMA FOR DIAGNOSIS
  • NONINFECTIOUS PRESENTATIONS SUGGESTING PIDD
  • Section 2. The T-, B-, and NK-Cell Systems
  • Chapter 165. T-Cell and Combined Deficiencies
  • T-CELL AND COMBINED DEFICIENCIES
  • 165.1. Severe Combined Immunodeficiencies
  • 165.2. Combined Immunodeficiencies
  • 165.3. Thymic Disorders
  • 165.4. Inborn Errors of Immunity with a Strong Atopic Diathesis
  • Chapter 166. B-Cell and Antibody Deficiencies
  • 166.1. Agammaglobulinemia
  • 166.2. Hypogammaglobulinemia, Transient Hypogammaglobulinemia of Infancy, Specific Antibody Deficiency, and Common Variable Immunodeficiency
  • 166.3. Class Switch Defects
  • 166.4. Isotype Defects
  • 166.5. Transient Hypogammaglobulinemia of Infancy
  • Chapter 167. Natural Killer Cells
  • NK CELL MARKERS, SUBSETS, AND MATURATION
  • NK CELL SPONTANEOUS CYTOTOXICITY
  • NK CELL ANTIBODY-DEPENDENT KILLING
  • FUNCTIONAL NK CELL DEFICIENCY (FNKCD)
  • FUNCTIONAL ASSAYS AVAILABLE FOR CLINICAL EVALUATION
  • NK CELL DEFICIENCY TREATMENT
  • Section 3. The Phagocytic System
  • Chapter 168. Neutrophils
  • THE PHAGOCYTIC INFLAMMATORY RESPONSE
  • HEMATOPOIESIS
  • NEUTROPHIL MATURATION AND KINETICS
  • NEUTROPHIL FUNCTION
  • Chapter 169. Eosinophils
  • DISEASES ASSOCIATED WITH EOSINOPHILIA
  • Chapter 170. Disorders of Phagocyte Function
  • LEUKOCYTE ADHESION DEFICIENCY
  • CHÉDIAK-HIGASHI SYNDROME
  • MYELOPEROXIDASE DEFICIENCY
  • CHRONIC GRANULOMATOUS DISEASE
  • Chapter 171. Leukopenia
  • NEUTROPENIA
  • LYMPHOPENIA
  • Chapter 172. Leukocytosis
  • NEUTROPHILIA
  • ADDITIONAL FORMS OF LEUKOCYTOSIS
  • Section 4. Complement System
  • Chapter 173. Complement System
  • 173.1. Complement Components, Pathways, and Evaluation
  • 173.2. Complement Pathway Deficiencies
  • Section 5. Immune Dysregulation
  • Chapter 174. Immune Dysregulation
  • 174.1. Tregopathies
  • 174.2. Hemophagocytic Lymphohistiocytosis
  • 174.3. Epstein-Barr Virus Susceptibility Disorders
  • 174.4. Chronic Active Epstein-Barr Virus
  • 174.5. Very Early Onset Inflammatory Bowel Disease
  • 174.6. Autoimmune Cytopenias
  • 174.7. Autoimmune Lymphoproliferative Syndrome
  • 174.8. Nuclear Factor-κB Pathway Defects
  • Chapter 175. Defects of Innate Immunity
  • 175.1. Predisposition to Fungal Infections
  • 175.2. Innate Immunity Defects with Predominant Susceptibility to Viral Infections
  • 175.3. Susceptibility to Invasive Bacterial Infections
  • 175.4. Mendelian Susceptibility to Mycobacterial Diseases
  • Chapter 176. Approaches to Treatment of Primary Immune Deficiency Diseases
  • GENERAL INFECTION PREVENTION AND MANAGEMENT STRATEGIES
  • IMMUNIZATIONS
  • GUIDANCE FOR CLOSE CONTACTS
  • COVID-19 VACCINE
  • PROPHYLAXIS
  • IMMUNODEFICIENCIES AFFECTING CELLULAR AND HUMORAL IMMUNITY
  • HYPER-IgM/CD40LG DEFICIENCY
  • COMBINED IMMUNODEFICIENCIES WITH ASSOCIATED OR SYNDROME FEATURES
  • STAT3 HYPER-IgE SYNDROME (JOB SYNDROME)
  • NF-κB ESSENTIAL MODULATOR (NEMO) DEFICIENCY
  • PREDOMINANTLY ANTIBODY DEFICIENCIES
  • CONGENITAL PHAGOCYTE DEFECTS
  • DEFECTS IN INTRINSIC AND INNATE IMMUNITY
  • COMPLEMENT DEFICIENCIES
  • IMMUNOGLOBULIN G REPLACEMENT THERAPY
  • INDICATIONS FOR IgRT
  • NORMAL IMMUNOGLOBULIN LEVELS WITH IMPAIRED SPECIFIC ANTIBODY PRODUCTION
  • INDIVIDUALIZING IgRT
  • CONSIDERATIONS FOR PRODUCT SELECTIONS
  • DOSING CONSIDERATIONS
  • ADMINISTRATION DETAILS
  • VACCINATION WHILE ON IgRT
  • Section 6. Hematopoietic Stem Cell Transplantation
  • Chapter 177. Principles and Clinical Indications of Hematopoietic Stem Cell Transplantation
  • HSCT FROM AN HLA–IDENTICAL SIBLING DONOR
  • ACUTE LYMPHOBLASTIC LEUKEMIA
  • ACUTE MYELOID LEUKEMIA
  • CHRONIC MYELOGENOUS LEUKEMIA
  • JUVENILE MYELOMONOCYTIC LEUKEMIA
  • MYELODYSPLASTIC SYNDROMES OTHER THAN JUVENILE MYELOMONOCYTIC LEUKEMIA
  • NON-HODGKIN LYMPHOMA AND HODGKIN DISEASE
  • ACQUIRED APLASTIC ANEMIA
  • INHERITED BONE MARROW FAILURE SYNDROMES
  • THALASSEMIA
  • SICKLE CELL DISEASE
  • IMMUNODEFICIENCY DISORDERS
  • INHERITED METABOLIC DISEASES
  • Chapter 178. Hematopoietic Stem Cell Transplantation from Alternative Sources and Donors
  • UNRELATED DONOR TRANSPLANTS
  • UMBILICAL CORD BLOOD TRANSPLANTS
  • HAPLOIDENTICAL TRANSPLANTS
  • DONOR VERSUS RECIPIENT NK CELL ALLOREACTIVITY
  • AUTOLOGOUS HEMATOPOIETIC STEM CELL TRANSPLANTATION
  • Chapter 179. Graft-Versus-Host Disease, Rejection, and Venoocclusive Disease
  • ACUTE GRAFT-VERSUS-HOST DISEASE
  • CHRONIC GRAFT-VERSUS-HOST DISEASE
  • GRAFT FAILURE
  • VENOOCCLUSIVE DISEASE
  • Chapter 180. Infectious Complications of Hematopoietic Stem Cell Transplantation
  • Chapter 181. Late Effects of Hematopoietic Stem Cell Transplantation
  • ENDOCRINE EFFECTS
  • CARDIOVASCULAR EFFECTS
  • SECONDARY MALIGNANCY
  • GRAFT-VERSUS-HOST DISEASE
  • OTHER EFFECTS
  • SPECIAL CONSIDERATIONS
  • Part XIII. Allergic Disorders
  • Chapter 182. Allergy and the Immunologic Basis of Atopic Disease
  • HYGIENE HYPOTHESIS
  • Biodiversity Hypothesis
  • Epithelial Barrier Hypothesis
  • KEY ELEMENTS OF ALLERGIC DISEASES
  • MECHANISMS OF ALLERGIC TISSUE INFLAMMATION
  • GENETIC BASIS OF ATOPY
  • Chapter 183. Diagnosis of Allergic Disease
  • ALLERGY HISTORY
  • PHYSICAL EXAMINATION
  • DIAGNOSTIC TESTING
  • Chapter 184. Allergic Rhinitis
  • ETIOLOGY AND CLASSIFICATION
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIFFERENTIAL DIAGNOSIS
  • COMPLICATIONS
  • LABORATORY FINDINGS
  • TREATMENT
  • PROGNOSIS
  • Chapter 185. Childhood Asthma
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS AND DIAGNOSIS
  • DIFFERENTIAL DIAGNOSIS
  • LABORATORY FINDINGS
  • TREATMENT
  • PROGNOSIS
  • PREVENTION
  • Chapter 186. Atopic Dermatitis (Atopic Eczema)
  • ETIOLOGY
  • PATHOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS
  • DIAGNOSIS AND DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • AVOIDING TRIGGERS
  • COMPLICATIONS
  • PROGNOSIS
  • PREVENTION
  • Chapter 187. Insect Allergy
  • ETIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PREVENTION
  • Chapter 188. Ocular Allergies
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • Chapter 189. Urticaria (Hives) and Angioedema
  • ETIOLOGY AND PATHOGENESIS
  • 189.1. Hereditary Angioedema
  • Chapter 190. Anaphylaxis
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS
  • DIAGNOSIS
  • TREATMENT
  • PREVENTION
  • Chapter 191. Serum Sickness
  • ETIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIFFERENTIAL DIAGNOSIS
  • DIAGNOSIS
  • TREATMENT
  • PREVENTION
  • Chapter 192. Food Allergy and Adverse Reactions to Foods
  • GENETIC AND ENVIRONMENTAL RISK FACTORS
  • 192.1. Non-IgE Gastrointestinal Food Allergy Disorders
  • Chapter 193. Adverse and Allergic Reactions to Drugs
  • EPIDEMIOLOGY
  • PATHOGENESIS AND CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • Part XIV. Rheumatic Diseases of Childhood (Connective Tissue Disease, Collagen Vascular Diseases)
  • Chapter 194. Evaluation of Suspected Rheumatic Disease
  • SYMPTOMS SUGGESTIVE OF RHEUMATIC DISEASE
  • SIGNS SUGGESTIVE OF RHEUMATIC DISEASE
  • LABORATORY TESTING
  • IMAGING STUDIES
  • Chapter 195. Treatment of Rheumatic Diseases
  • PEDIATRIC RHEUMATOLOGY TEAMS AND PRIMARY CARE PHYSICIANS
  • THERAPEUTICS
  • JANUS KINASE INHIBITORS
  • Chapter 196. Juvenile Idiopathic Arthritis
  • EPIDEMIOLOGY
  • ETIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • DIFFERENTIAL DIAGNOSIS
  • LABORATORY FINDINGS
  • TREATMENT
  • PROGNOSIS
  • Chapter 197. Ankylosing Spondylitis and Other Spondyloarthritides
  • EPIDEMIOLOGY
  • ETIOLOGY AND PATHOGENESIS
  • CLINICAL MANIFESTATIONS AND DIAGNOSIS
  • LABORATORY FINDINGS
  • DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • Chapter 198. Reactive and Postinfectious Arthritis
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS AND DIFFERENTIAL DIAGNOSIS
  • DIAGNOSIS
  • TREATMENT
  • COMPLICATIONS AND PROGNOSIS
  • Chapter 199. Systemic Lupus Erythematosus
  • ETIOLOGY
  • 199.1. Neonatal Lupus
  • Chapter 200. Juvenile Dermatomyositis
  • EPIDEMIOLOGY
  • ETIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • DIFFERENTIAL DIAGNOSIS
  • LABORATORY FINDINGS
  • TREATMENT
  • COMPLICATIONS
  • PROGNOSIS
  • Chapter 201. Scleroderma and Raynaud Phenomenon
  • ETIOLOGY AND PATHOGENESIS
  • CLASSIFICATION
  • EPIDEMIOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • Chapter 202. Behçet Disease
  • EPIDEMIOLOGY
  • ETIOLOGY AND PATHOGENESIS
  • CLINICAL MANIFESTATIONS AND DIAGNOSIS
  • TREATMENT AND PROGNOSIS
  • Chapter 203. Sjögren Syndrome
  • EPIDEMIOLOGY
  • ETIOLOGY AND PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • COMPLICATIONS AND PROGNOSIS
  • Chapter 204. Hereditary Periodic Fever Syndromes and Other Systemic Autoinflammatory Diseases
  • CLASSIFICATION OF AUTOINFLAMMATORY DISORDERS
  • AUTOINFLAMMATORY DISEASES WITH PERIODIC OR PROMINENT FEVERS
  • OTHER MENDELIAN AUTOINFLAMMATORY DISEASES
  • GENETICALLY COMPLEX AUTOINFLAMMATORY DISEASES
  • Chapter 205. Interferonopathies
  • AUTOINFLAMMATORY INTERFERONOPATHIES
  • AUTOIMMUNE INTERFERONOPATHIES
  • Chapter 206. Amyloidosis
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • LABORATORY FINDINGS
  • TREATMENT
  • PROGNOSIS
  • PREVENTION
  • Chapter 207. Macrophage Activation Syndrome
  • EPIDEMIOLOGY
  • PATHOPHYSIOLOGY AND OTHER HYPERINFLAMMATORY SYNDROMES
  • CLINICAL AND LABORATORY MANIFESTATIONS
  • DIAGNOSIS
  • DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • Chapter 208. Kawasaki Disease
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOLOGY
  • CLINICAL MANIFESTATIONS
  • LABORATORY AND RADIOLOGY FINDINGS
  • DIAGNOSIS
  • DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • COMPLICATIONS
  • PROGNOSIS
  • Chapter 209. Sarcoidosis
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOLOGY AND PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS
  • DIAGNOSIS
  • DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • Chapter 210. Vasculitis Syndromes
  • INTRODUCTION
  • 210.1. Henoch-Schönlein Purpura (IgA Vasculitis)
  • 210.2. Takayasu Arteritis
  • 210.3. Polyarteritis Nodosa and Cutaneous Polyarteritis Nodosa
  • 210.4. Antineutrophilic Cytoplasmic Antibody–Associated Vasculitis
  • 210.5. Other Vasculitis Syndromes: Hypersensitivity, CNS, and COVID-19 Related
  • Chapter 211. Musculoskeletal Pain Syndromes
  • CLINICAL MANIFESTATIONS
  • 211.1. Growing Pains (Benign Limb Pain of Childhood)
  • 211.2. Small Fiber Polyneuropathy
  • 211.3. Diffuse Amplified Pain Syndromes
  • 211.4. Complex Regional Pain Syndrome
  • 211.5. Erythromelalgia
  • Chapter 212. Chronic Overlapping Pain Conditions
  • PREVALENCE
  • 212.1. Chronic Fatigue Syndrome
  • Chapter 213. Miscellaneous Conditions Associated with Arthritis
  • RELAPSING POLYCHONDRITIS
  • MUCHA-HABERMANN DISEASE/PITYRIASIS LICHENOIDES ET VARIOLIFORMIS ACUTA
  • SWEET SYNDROME
  • HYPERTROPHIC OSTEOARTHROPATHY
  • PLANT THORN SYNOVITIS
  • PIGMENTED VILLONODULAR SYNOVITIS
  • Infectious Diseases
  • Section 1. General Considerations
  • Chapter 214. Public Health Approach to Pandemics
  • INTRODUCTION
  • DEFINITIONS
  • Section 2. Preventive Measures
  • Chapter 215. Immunization Practices
  • PASSIVE IMMUNITY
  • 215.1. International Immunization Practices
  • Chapter 216. Infection Prevention and Control
  • TRANSMISSION IN THE HEALTHCARE SETTING
  • PREVENTION STRATEGIES
  • ENVIRONMENT, DISINFECTION, AND STERILIZATION
  • VISITATION AND PATIENT AND CAREGIVER MANAGEMENT
  • OCCUPATIONAL HEALTH AND CLINICIAN EDUCATION
  • SPECIAL POPULATIONS
  • Chapter 217. Childcare and Communicable Diseases
  • EPIDEMIOLOGY
  • RESPIRATORY TRACT INFECTIONS
  • GASTROINTESTINAL TRACT INFECTIONS
  • SKIN DISEASES
  • INVASIVE ORGANISMS AND SYSTEMIC INFECTIONS
  • HERPESVIRUSES
  • BLOOD-BORNE PATHOGENS
  • ANTIBIOTIC USE AND BACTERIAL RESISTANCE
  • PREVENTION
  • STANDARDS
  • Chapter 218. Health Advice for Children Traveling Internationally
  • THE PEDIATRIC TRAVEL MEDICINE CONSULTATION
  • SAFETY AND PREVENTIVE COUNSELING TOPICS
  • ROUTINE CHILDHOOD VACCINATIONS REQUIRED FOR PEDIATRIC TRAVEL
  • SPECIALIZED PEDIATRIC TRAVEL VACCINATIONS
  • TRAVELER’S DIARRHEA
  • INSECT-BORNE INFECTIONS
  • MALARIA CHEMOPROPHYLAXIS
  • THE RETURNING TRAVELER
  • THE ADOLESCENT TRAVELER
  • Chapter 219. Fever
  • PATHOGENESIS
  • ETIOLOGY
  • CLINICAL FEATURES
  • EVALUATION
  • MANAGEMENT
  • Chapter 220. Fever Without a Focus in the Neonate and Young Infant
  • ETIOLOGY AND EPIDEMIOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • LABORATORY DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • Chapter 221. Fever in the Older Child
  • DIAGNOSIS
  • GENERAL APPROACH
  • EVALUATION
  • MANAGEMENT
  • Chapter 222. Fever of Unknown Origin
  • ETIOLOGY
  • DIAGNOSIS
  • MANAGEMENT
  • PROGNOSIS
  • Chapter 223. Infections in Immunocompromised Persons
  • 223.1. Infections Occurring with Primary Immunodeficiencies
  • 223.2. Infections Occurring with Acquired Immunodeficiencies
  • 223.3. Prevention of Infection in Immunocompromised Persons
  • Chapter 224. Infection Associated with Medical Devices
  • INTRAVASCULAR ACCESS DEVICES
  • URINARY CATHETERS
  • MECHANICAL VENTILATORS
  • CEREBROSPINAL FLUID SHUNTS
  • PERITONEAL DIALYSIS CATHETERS
  • IMPLANTABLE ORTHOPEDIC DEVICES
  • Section 3. Antibiotic Therapy
  • Chapter 225. Principles of Antibacterial Therapy
  • AGE- AND RISK-SPECIFIC USE OF ANTIBIOTICS IN CHILDREN
  • ANTIBIOTICS, INCLUDING NEWER AGENTS AND THERAPIES COMMONLY USED IN PEDIATRIC PRACTICE
  • Chapter 226. Antimicrobial Stewardship
  • THE NEED FOR ANTIMICROBIAL STEWARDSHIP: HARMS FROM OVERUSE
  • DEFINING ANTIMICROBIAL STEWARDSHIP AND AN ANTIMICROBIAL STEWARDSHIP PROGRAM
  • INPATIENT ANTIMICROBIAL STEWARDSHIP STRATEGIES
  • OUTPATIENT ANTIMICROBIAL STEWARDSHIP STRATEGIES
  • TRACKING AND REPORTING ANTIMICROBIAL USE MEASURES
  • Section 4. Gram-Positive Bacterial Infections
  • Chapter 227. Staphylococcus
  • 227.1. Staphylococcus aureus
  • 227.2. Toxic Shock Syndrome
  • 227.3. Coagulase-Negative Staphylococci
  • Chapter 228. Streptococcus pneumoniae (Pneumococcus)
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • PREVENTION
  • Chapter 229. Group A Streptococcus
  • ETIOLOGY
  • 229.1. Rheumatic Fever
  • Chapter 230. Group B Streptococcus
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • LABORATORY FINDINGS
  • TREATMENT
  • PROGNOSIS
  • PREVENTION
  • Chapter 231. Non–Group A or B Streptococci
  • Chapter 232. Enterococcus
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • TREATMENT
  • PREVENTION
  • Chapter 233. Diphtheria (Corynebacterium diphtheriae)
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • COMPLICATIONS
  • TREATMENT
  • SUPPORTIVE CARE
  • PROGNOSIS
  • PREVENTION
  • Chapter 234. Listeria monocytogenes
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • PREVENTION
  • Acknowledgments
  • Chapter 235. Actinomyces
  • TAXONOMY AND MICROBIOLOGY
  • PATHOGENESIS AND EPIDEMIOLOGY
  • DIAGNOSIS
  • COMMON CLINICAL PRESENTATIONS
  • DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • Chapter 236. Nocardia
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL AND RADIOGRAPHIC MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • Section 5. Gram-Negative Bacterial Infections
  • Chapter 237. Neisseria meningitidis (Meningococcus)
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS AND PATHOPHYSIOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • COMPLICATIONS
  • PROGNOSIS
  • PREVENTION
  • Chapter 238. Neisseria gonorrhoeae (Gonococcus)
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS AND PATHOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • COMPLICATIONS
  • PREVENTION
  • Chapter 239. Kingella kingae
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL DISEASE
  • SPONDYLODISCITIS
  • DIAGNOSIS
  • TREATMENT
  • PREVENTION
  • Chapter 240. Haemophilus influenzae
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • DIAGNOSIS
  • CLINICAL MANIFESTATIONS AND TREATMENT
  • PREVENTION
  • Chapter 241. Chancroid (Haemophilus ducreyi)
  • ETIOLOGY AND EPIDEMIOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • COMPLICATIONS
  • Chapter 242. Moraxella catarrhalis
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS OF INFECTION
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PREVENTION
  • Chapter 243. Pertussis (Bordetella pertussis and Bordetella parapertussis)
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • COMPLICATIONS
  • PREVENTION
  • Chapter 244. Salmonella
  • 244.1. Nontyphoidal Salmonellosis
  • 244.2. Enteric Fever (Typhoid and Paratyphoid Fever)
  • Chapter 245. Shigella
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • IMMUNITY
  • CLINICAL MANIFESTATIONS AND COMPLICATIONS
  • DIFFERENTIAL DIAGNOSIS
  • DIAGNOSIS
  • TREATMENT
  • PREVENTION
  • Chapter 246. Escherichia coli
  • ENTEROTOXIGENIC ESCHERICHIA COLI
  • ENTEROINVASIVE ESCHERICHIA COLI
  • ENTEROPATHOGENIC ESCHERICHIA COLI
  • ENTEROAGGREGATIVE ESCHERICHIA COLI
  • SHIGA TOXIN–PRODUCING ESCHERICHIA COLI
  • ENTEROAGGREGATIVE HEMORRHAGIC ESCHERICHIA COLI
  • DIFFUSELY ADHERENT ESCHERICHIA COLI
  • DIAGNOSIS
  • TREATMENT
  • PREVENTION OF ILLNESS
  • Chapter 247. Cholera
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS
  • DIAGNOSIS AND DIFFERENTIAL DIAGNOSIS
  • COMPLICATIONS
  • TREATMENT
  • PREVENTION
  • Chapter 248. Campylobacter
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • COMPLICATIONS
  • PROGNOSIS
  • PREVENTION
  • Chapter 249. Yersinia
  • 249.1. Yersinia enterocolitica
  • 249.2. Yersinia pseudotuberculosis
  • 249.3. Plague (Yersinia pestis)
  • Chapter 250. Aeromonas and Plesiomonas
  • 250.1. Aeromonas
  • 250.2. Plesiomonas shigelloides
  • Chapter 251. Pseudomonas, Burkholderia, and Stenotrophomonas
  • 251.1. Pseudomonas aeruginosa
  • 251.2. Burkholderia cepacia Complex
  • 251.3. Stenotrophomonas
  • Chapter 252. Tularemia (Francisella tularensis)
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • PREVENTION
  • Chapter 253. Brucella
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • PREVENTION
  • Chapter 254. Legionella
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • Chapter 255. Bartonella
  • 255.1
  • 255.1. Cat Scratch Disease (Bartonella henselae)
  • 255.2. Bartonellosis (Bartonella bacilliformis)
  • 255.3. Trench Fever (Bartonella quintana)
  • 255.4. Bacillary Angiomatosis and Bacillary Peliosis Hepatis (Bartonella henselae and Bartonella quintana)
  • Section 6. Anaerobic Bacterial Infections
  • Chapter 256. Botulism (Clostridium botulinum)
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • SUPPORTIVE CARE
  • COMPLICATIONS
  • PROGNOSIS
  • PREVENTION
  • Chapter 257. Tetanus (Clostridium tetani)
  • ETIOLOGY
  • EPIDEMIOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • SUPPORTIVE CARE
  • COMPLICATIONS
  • PROGNOSIS
  • PREVENTION
  • Chapter 258. Clostridioides difficile Infection
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PROGNOSIS AND RECURRENCE
  • PREVENTION
  • Chapter 259. Other Anaerobic Infections
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • ANAEROBIC GRAM-NEGATIVE BACILLI
  • ANAEROBIC GRAM-POSITIVE ORGANISMS
  • Section 7. Mycobacterial Infections
  • Chapter 260. Principles of Antimycobacterial Therapy
  • AGENTS USED AGAINST MYCOBACTERIUM TUBERCULOSIS
  • AGENTS USED AGAINST MYCOBACTERIUM LEPRAE
  • AGENTS USED AGAINST NONTUBERCULOUS MYCOBACTERIA
  • Chapter 261. Tuberculosis (Mycobacterium tuberculosis)
  • CLINICAL STAGES
  • EPIDEMIOLOGY
  • TRANSMISSION
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • IMMUNE-BASED TESTING (“TESTS OF TUBERCULOSIS INFECTION”)
  • MYCOBACTERIAL SAMPLING, SUSCEPTIBILITY, AND CULTURE
  • TREATMENT
  • PREVENTION
  • Chapter 262. Hansen Disease (Mycobacterium leprae)
  • MICROBIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • DISEASE CLASSIFICATION
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • LONG-TERM COMPLICATIONS
  • PREVENTION
  • Chapter 263. Nontuberculous Mycobacteria
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • Section 8. Spirochetal Infections
  • Chapter 264. Syphilis (Treponema pallidum)
  • ETIOLOGY
  • EPIDEMIOLOGY
  • CLINICAL MANIFESTATIONS AND LABORATORY FINDINGS
  • DIAGNOSIS
  • TREATMENT
  • PREVENTION
  • Chapter 265. Nonvenereal Treponemal Infections
  • 265.1. Yaws (Treponema pertenue)
  • 265.2. Bejel (Endemic Syphilis; Treponema pallidum endemicum)
  • 265.3. Pinta (Treponema carateum)
  • Chapter 266. Leptospira
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOLOGY AND PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PREVENTION
  • Chapter 267. Relapsing Fever (Borrelia)
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOLOGY AND PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • PREVENTION
  • Chapter 268. Lyme Disease (Borrelia burgdorferi)
  • ETIOLOGY
  • TRANSMISSION
  • EPIDEMIOLOGY
  • PATHOLOGY AND PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS
  • DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • PREVENTION
  • Section 9. Mycoplasmal Infections
  • Chapter 269. Mycoplasma pneumoniae
  • THE ORGANISM
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PREVENTION
  • Chapter 270. Genital Mycoplasmas (Mycoplasma hominis, Mycoplasma genitalium, and Ureaplasma urealyticum)
  • ETIOLOGY
  • EPIDEMIOLOGY
  • TRANSMISSION
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • Section 10. Chlamydial Infections
  • Chapter 271. Chlamydia pneumoniae
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • Chapter 272. Chlamydia trachomatis
  • 272.1. Trachoma
  • 272.2. Genital Tract Infections
  • 272.3. Conjunctivitis and Pneumonia in Newborns
  • 272.4. Lymphogranuloma Venereum
  • Chapter 273. Psittacosis (Chlamydia psittaci)
  • ETIOLOGY
  • EPIDEMIOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • PREVENTION
  • Section 11. Rickettsial Infections
  • Chapter 274. Spotted Fever Group Rickettsioses
  • Introduction
  • 274.1. Rocky Mountain Spotted Fever (Rickettsia rickettsii)
  • 274.2. Mediterranean Spotted Fever or Boutonneuse Fever (Rickettsia conorii)
  • 274.3. Rickettsialpox (Rickettsia akari) and Flea-Borne Spotted Fever
  • Chapter 275. Scrub Typhus (Orientia tsutsugamushi)
  • ETIOLOGY
  • EPIDEMIOLOGY
  • TRANSMISSION
  • PATHOLOGY AND PATHOGENESIS
  • CLINICAL MANIFESTATIONS AND LABORATORY FINDINGS
  • DIAGNOSIS AND DIFFERENTIAL DIAGNOSIS
  • TREATMENT AND SUPPORTIVE CARE
  • COMPLICATIONS
  • PREVENTION
  • Chapter 276. Typhus Group Rickettsioses
  • 276.1. Murine (Endemic or Flea-Borne) Typhus (Rickettsia typhi)
  • 276.2. Epidemic (Louse-Borne) Typhus (Rickettsia prowazekii)
  • Chapter 277. Ehrlichiosis and Anaplasmosis
  • ETIOLOGY
  • EPIDEMIOLOGY
  • TRANSMISSION
  • PATHOLOGY AND PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS
  • DIAGNOSIS
  • DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • COMPLICATIONS AND PROGNOSIS
  • PREVENTION
  • Chapter 278. Q Fever (Coxiella burnetii)
  • ETIOLOGY
  • EPIDEMIOLOGY
  • TRANSMISSION
  • PATHOLOGY AND PATHOGENESIS
  • CLINICAL MANIFESTATIONS AND COMPLICATIONS
  • LABORATORY FINDINGS
  • DIAGNOSIS AND DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • PREVENTION
  • Section 12. Fungal Infections
  • Chapter 279. Principles of Antifungal Therapy
  • POLYENES
  • PYRIMIDINE ANALOGS
  • AZOLES
  • ECHINOCANDINS
  • Chapter 280. Candida
  • 280.1. Neonatal Infections
  • 280.2. Infections in Immunocompetent Children and Adolescents
  • 280.3. Infections in Immunocompromised Children and Adolescents
  • Chapter 281. Cryptococcus neoformans and Cryptococcus gattii
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PREVENTION
  • Chapter 282. Malassezia
  • Chapter 283. Aspergillus
  • 283.1. Allergic Disease (Hypersensitivity Syndromes)
  • 283.2. Saprophytic (Noninvasive) Syndromes
  • 283.3. Invasive Disease
  • Chapter 284. Histoplasmosis (Histoplasma capsulatum)
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • Chapter 285. Blastomycosis
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • Chapter 286. Coccidioidomycosis (Coccidioides Species)
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PREVENTION
  • Chapter 287. Paracoccidioides brasiliensis
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • Chapter 288. Sporotrichosis (Sporothrix schenckii)
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • Chapter 289. Mucormycosis
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • Chapter 290. Pneumocystis jirovecii
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • PATHOLOGY
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS AND DIAGNOSIS
  • TREATMENT
  • SUPPORTIVE CARE
  • COMPLICATIONS
  • PROGNOSIS
  • PREVENTION
  • Chapter 291. Other Pathogenic Fungi
  • PHAEOHYPHOMYCOSIS: Cladophialophora bantiana, Bipolaris spp., AND OTHERS
  • HYALOHYPHOMYCOSIS: Fusarium AND Scedosporium spp. AND OTHERS
  • Section 13. Viral Infections
  • Chapter 292. Principles of Antiviral Therapy
  • ANTIVIRALS USED FOR HERPESVIRUSES
  • ANTIVIRALS USED FOR RESPIRATORY VIRAL INFECTIONS
  • ANTIVIRALS USED FOR COVID-19
  • ANTIVIRALS USED FOR HEPATITIS
  • ANTIVIRAL IMMUNE GLOBULINS
  • Chapter 293. Measles
  • ETIOLOGY
  • EPIDEMIOLOGY
  • TRANSMISSION
  • PATHOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • MODIFIED MEASLES INFECTION
  • LABORATORY FINDINGS
  • DIAGNOSIS
  • DIFFERENTIAL DIAGNOSIS
  • COMPLICATIONS
  • TREATMENT
  • PROGNOSIS
  • PREVENTION
  • Chapter 294. Rubella
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS
  • DIAGNOSES
  • DIFFERENTIAL DIAGNOSES
  • COMPLICATIONS
  • TREATMENT
  • SUPPORTIVE CARE
  • PROGNOSIS
  • PREVENTION
  • VACCINATION
  • Chapter 295. Mumps
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOLOGY AND PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • DIFFERENTIAL DIAGNOSIS
  • COMPLICATIONS
  • TREATMENT
  • PROGNOSIS
  • PREVENTION
  • Chapter 296. Polioviruses
  • ETIOLOGY
  • EPIDEMIOLOGY
  • TRANSMISSION
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • COMPLICATIONS
  • PROGNOSIS
  • PREVENTION
  • Chapter 297. Nonpolio Enteroviruses
  • ETIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • COMPLICATIONS AND PROGNOSIS
  • Chapter 298. Parvoviruses
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • COMPLICATIONS
  • PREVENTION
  • Chapter 299. Herpes Simplex Virus
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • LABORATORY FINDINGS
  • TREATMENT AND PREVENTION
  • PROGNOSIS
  • PREVENTION
  • Chapter 300. Varicella-Zoster Virus
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • COMPLICATIONS
  • DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • PREVENTION
  • Chapter 301. Epstein-Barr Virus
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • COMPLICATIONS
  • ONCOGENESIS
  • TREATMENT
  • PROGNOSIS
  • PREVENTION
  • Chapter 302. Cytomegalovirus
  • THE VIRUS AND ITS HOST INTERACTIONS
  • EPIDEMIOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PREVENTION
  • Chapter 303. Roseola (Human Herpesviruses 6 and 7)
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOLOGY AND PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS
  • DIAGNOSIS
  • COMPLICATIONS
  • TREATMENT
  • PROGNOSIS
  • PREVENTION
  • Chapter 304. Human Herpesvirus 8
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOLOGY AND PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • Chapter 305. Influenza Viruses
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • COMPLICATIONS
  • LABORATORY FINDINGS
  • DIAGNOSIS AND DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • SUPPORTIVE CARE
  • PROGNOSIS
  • PREVENTION
  • Chapter 306. Parainfluenza Viruses
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS AND DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • COMPLICATIONS
  • PROGNOSIS
  • PREVENTION
  • Chapter 307. Respiratory Syncytial Virus
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • PREVENTION
  • Chapter 308. Human Metapneumovirus
  • ETIOLOGY
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS
  • DIAGNOSIS AND DIFFERENTIAL DIAGNOSIS
  • COMPLICATIONS
  • TREATMENT
  • PROGNOSIS
  • PREVENTION
  • Chapter 309. Adenoviruses
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • COMPLICATIONS
  • TREATMENT
  • PREVENTION
  • Chapter 310. Rhinoviruses
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • COMPLICATIONS
  • TREATMENT
  • PREVENTION
  • Chapter 311. Coronaviruses
  • ETIOLOGY
  • 311.1. COVID-19
  • Chapter 312. Rotaviruses, Caliciviruses, and Astroviruses
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • LABORATORY FINDINGS
  • DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • PREVENTION
  • Chapter 313. Human Papillomaviruses
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • COMPLICATIONS
  • PROGNOSIS
  • PREVENTION
  • Chapter 314. Arboviral Infections
  • ETIOLOGY
  • 314.1. Eastern Equine Encephalitis
  • 314.2. Western Equine Encephalitis
  • 314.3. St. Louis Encephalitis
  • 314.4. West Nile Encephalitis
  • 314.5. Powassan Encephalitis
  • 314.6. La Crosse and California Encephalitis
  • 314.7. Colorado Tick Fever
  • 314.8. Chikungunya Fever
  • 314.9. Venezuelan Equine Encephalitis
  • 314.10. Japanese Encephalitis
  • 314.11. Tick-Borne Encephalitis
  • 314.12. Zika Virus
  • Chapter 315. Dengue Fever, Dengue Hemorrhagic Fever, and Severe Dengue
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • DIFFERENTIAL DIAGNOSIS
  • LABORATORY FINDINGS
  • TREATMENT
  • COMPLICATIONS
  • PROGNOSIS
  • PREVENTION
  • Chapter 316. Yellow Fever
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • COMPLICATIONS
  • PREVENTION
  • Chapter 317. Ebola and Other Viral Hemorrhagic Fevers
  • ETIOLOGY
  • EPIDEMIOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PREVENTION
  • Chapter 318. Lymphocytic Choriomeningitis Virus
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS
  • DIAGNOSIS AND DIFFERENTIAL DIAGNOSIS
  • COMPLICATIONS
  • TREATMENT
  • PROGNOSIS
  • PREVENTION
  • Chapter 319. Hantavirus Pulmonary Syndrome
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • PREVENTION
  • Chapter 320. Rabies
  • EPIDEMIOLOGY
  • TRANSMISSION
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIFFERENTIAL DIAGNOSIS
  • DIAGNOSIS
  • TREATMENT AND PROGNOSIS
  • PREVENTION
  • Chapter 321. Polyomaviruses
  • GENOMIC ORGANIZATION
  • PyV EPIDEMIOLOGY
  • BK PyV
  • JC PyV
  • Chapter 322. Human Immunodeficiency Virus and Acquired Immunodeficiency Syndrome
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS AND TESTING
  • TREATMENT
  • PROGNOSIS
  • PREVENTION
  • SUMMARY
  • Chapter 323. Human T-Cell Leukemia Viruses (1 and 2)
  • ETIOLOGY
  • EPIDEMIOLOGY AND MODES OF TRANSMISSION
  • DIAGNOSIS
  • CLINICAL MANIFESTATIONS
  • ADULT T-CELL LEUKEMIA/LYMPHOMA
  • HUMAN T-CELL LYMPHOTROPIC VIRUS-1–ASSOCIATED MYELOPATHY
  • HUMAN T-CELL LYMPHOTROPIC VIRUS-2
  • PREVENTION
  • Chapter 324. Transmissible Spongiform Encephalopathies
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS AND PATHOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • LABORATORY FINDINGS
  • TREATMENT
  • GENETIC COUNSELING
  • PROGNOSIS
  • FAMILY SUPPORT
  • PREVENTION
  • Section 14. Antiparasitic Therapy
  • Chapter 325. Principles of Antiparasitic Therapy
  • SELECTED ANTIPARASITIC DRUGS FOR PROTOZOANS
  • SELECTED ANTIPARASITIC DRUGS FOR HELMINTHS AND ECTOPARASITES
  • Section 15. Protozoan Diseases
  • Chapter 326. Primary Amebic Meningoencephalitis
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • Chapter 327. Amebiasis
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS
  • DIAGNOSIS AND DIFFERENTIAL DIAGNOSIS
  • COMPLICATIONS
  • TREATMENT
  • PROGNOSIS
  • PREVENTION
  • Chapter 328. Giardiasis and Balantidiasis
  • 328.1. Giardia duodenalis
  • 328.2. Balantidiasis
  • Chapter 329. Cryptosporidium, Cystoisospora, Cyclospora, and Microsporidia
  • CRYPTOSPORIDIUM
  • Diagnosis
  • CYSTOISOSPORA
  • CYCLOSPORA
  • MICROSPORIDIA
  • Chapter 330. Trichomoniasis (Trichomonas vaginalis)
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • COMPLICATIONS
  • TREATMENT
  • PREVENTION
  • Chapter 331. Leishmaniasis (Leishmania)
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS
  • DIFFERENTIAL DIAGNOSIS
  • DIAGNOSIS
  • TREATMENT
  • PREVENTION
  • Chapter 332. African Trypanosomiasis (Sleeping Sickness; Trypanosoma brucei Complex)
  • ETIOLOGY
  • LIFE CYCLE
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PREVENTION
  • Chapter 333. American Trypanosomiasis (Chagas Disease; Trypanosoma cruzi)
  • ETIOLOGY
  • LIFE CYCLE
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PREVENTION
  • Chapter 334. Malaria (Plasmodium)
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • TREATMENT OF UNCOMPLICATED MALARIA
  • TREATMENT OF SEVERE MALARIA
  • FOLLOW-UP ORAL ANTIMALARIAL THERAPY FOR SEVERE MALARIA
  • PREVENTION
  • Chapter 335. Babesiosis (Babesia)
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • PREVENTION
  • Chapter 336. Toxoplasmosis (Toxoplasma gondii)
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • SYSTEMIC SIGNS
  • DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • PREVENTION
  • Acknowledgment
  • Section 16. Helminthic Diseases
  • Chapter 337. Ascariasis (Ascaris lumbricoides)
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PREVENTION
  • Chapter 338. Hookworms (Necator americanus and Ancylostoma spp.)
  • ETIOLOGY
  • 338.1. Cutaneous Larva Migrans
  • Chapter 339. Trichuriasis (Trichuris trichiura)
  • ETIOLOGY
  • EPIDEMIOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PREVENTION
  • Chapter 340. Enterobiasis (Enterobius vermicularis)
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PREVENTION
  • Chapter 341. Strongyloidiasis (Strongyloides stercoralis)
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PREVENTION
  • Chapter 342. Lymphatic Filariasis (Brugia malayi, Brugia timori, and Wuchereria bancrofti)
  • ETIOLOGY
  • EPIDEMIOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • Chapter 343. Other Tissue Nematodes
  • ONCHOCERCIASIS (ONCHOCERCA VOLVULUS)
  • LOIASIS (LOA LOA)
  • INFECTION WITH ANIMAL FILARIAE
  • ANGIOSTRONGYLUS CANTONENSIS
  • ANGIOSTRONGYLUS COSTARICENSIS
  • DRACUNCULIASIS (DRACUNCULUS MEDINENSIS)
  • GNATHOSTOMA SPINIGERUM
  • Chapter 344. Toxocariasis (Visceral and Ocular Larva Migrans)
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PREVENTION
  • Chapter 345. Trichinellosis (Trichinella spiralis)
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PREVENTION
  • Chapter 346. Schistosomiasis (Schistosoma)
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PREVENTION
  • Chapter 347. Flukes (Liver, Lung, and Intestinal)
  • LIVER FLUKES
  • LUNG FLUKES
  • INTESTINAL FLUKES
  • Chapter 348. Adult Tapeworm Infections
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • PREVENTION
  • DIPHYLLOBOTHRIASIS (DIBOTHRIOCEPHALUS SPP.)
  • HYMENOLEPIASIS (HYMENOLEPIS)
  • DIPYLIDIASIS (DIPYLIDIUM CANINUM)
  • Chapter 349. Cysticercosis
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PREVENTION
  • Chapter 350. Echinococcosis (Echinococcus granulosus sensu lato and Echinococcus multilocularis)
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • PREVENTION
  • Volume 2
  • The Digestive System
  • Section 1. Clinical Manifestations of Gastrointestinal Disease
  • Chapter 351. Normal Digestive Tract Phenomena
  • Chapter 352. Major Symptoms and Signs of Digestive Tract Disorders
  • DYSPHAGIA
  • REGURGITATION
  • NAUSEA
  • VOMITING
  • DIARRHEA
  • CONSTIPATION
  • ANOREXIA
  • ABDOMINAL PAIN
  • GASTROINTESTINAL HEMORRHAGE
  • ABDOMINAL DISTENTION AND ABDOMINAL MASSES
  • ACKNOWLEDGMENT
  • Section 2. The Oral Cavity
  • Chapter 353. Development and Developmental Anomalies of the Teeth
  • DEVELOPMENT OF TEETH
  • Chapter 354. Disorders of the Oral Cavity Associated with Other Conditions
  • Chapter 355. Malocclusion
  • VARIATIONS IN GROWTH PATTERNS
  • CROSSBITE
  • OPEN AND CLOSED BITES
  • DENTAL CROWDING
  • DIGIT SUCKING
  • Chapter 356. Cleft Lip and Palate
  • INCIDENCE AND EPIDEMIOLOGY
  • CLINICAL MANIFESTATIONS
  • TREATMENT
  • POSTOPERATIVE MANAGEMENT
  • SEQUELAE
  • VELOPHARYNGEAL DYSFUNCTION
  • Chapter 357. Syndromes with Oral Manifestations
  • Chapter 358. Dental Caries
  • ETIOLOGY
  • EPIDEMIOLOGY
  • CLINICAL MANIFESTATIONS
  • COMPLICATIONS
  • TREATMENT
  • PREVENTION
  • Chapter 359. Periodontal Diseases
  • GINGIVITIS
  • AGGRESSIVE PERIODONTITIS IN CHILDREN (PREPUBERTAL PERIODONTITIS)
  • AGGRESSIVE PERIODONTITIS IN ADOLESCENTS
  • CYCLOSPORINE- OR PHENYTOIN-INDUCED GINGIVAL OVERGROWTH
  • ACUTE PERICORONITIS
  • NECROTIZING PERIODONTAL DISEASE (ACUTE NECROTIZING ULCERATIVE GINGIVITIS)
  • Chapter 360. Dental Trauma
  • INJURIES TO TEETH
  • INJURIES TO PERIODONTAL STRUCTURES
  • PREVENTION
  • ADDITIONAL CONSIDERATIONS
  • Chapter 361. Common Lesions of the Oral Soft Tissues
  • OROPHARYNGEAL CANDIDIASIS
  • APHTHOUS ULCERS
  • HERPETIC GINGIVOSTOMATITIS
  • RECURRENT HERPES LABIALIS
  • PARULIS
  • CHEILITIS
  • ANKYLOGLOSSIA
  • GEOGRAPHIC TONGUE
  • FISSURED TONGUE
  • DEVELOPMENTAL (NORMAL) VARIATIONS
  • Chapter 362. Diseases of the Salivary Glands and Jaws
  • PAROTITIS
  • RANULA
  • MUCOCELE
  • CONGENITAL LIP PITS
  • ERUPTION CYST
  • XEROSTOMIA
  • SALIVARY GLAND TUMORS
  • HISTIOCYTIC DISORDERS
  • TUMORS OF THE JAW
  • Chapter 363. Diagnostic Radiology in Dental Assessment
  • Section 3. The Esophagus
  • Chapter 364. Embryology, Anatomy, and Function of the Esophagus
  • EMBRYOLOGY
  • 364.1. Common Clinical Manifestations and Diagnostic Aids
  • Chapter 365. Congenital Anomalies
  • 365.1. Esophageal Atresia and Tracheoesophageal Fistula
  • 365.2. Laryngotracheoesophageal Clefts
  • 365.3. Congenital Esophageal Stenosis
  • Chapter 366. Obstructing Disorders of the Esophagus
  • EXTRINSIC
  • INTRINSIC
  • Chapter 367. Dysmotility
  • UPPER ESOPHAGEAL AND UPPER ESOPHAGEAL SPHINCTER DYSMOTILITY (STRIATED MUSCLE)
  • LOWER ESOPHAGEAL AND LOWER ESOPHAGEAL SPHINCTER DYSFUNCTION (SMOOTH MUSCLE)
  • Chapter 368. Hiatal Hernia
  • Chapter 369. Gastroesophageal Reflux Disease
  • PATHOPHYSIOLOGY
  • 369.1. Complications of Gastroesophageal Reflux Disease
  • Chapter 370. Eosinophilic Esophagitis, Pill Esophagitis, and Infective Esophagitis
  • EOSINOPHILIC ESOPHAGITIS
  • INFECTIVE ESOPHAGITIS
  • PILL ESOPHAGITIS
  • Chapter 371. Esophageal Perforation
  • Chapter 372. Esophageal Varices
  • Chapter 373. Ingestions
  • 373.1. Foreign Bodies in the Esophagus
  • 373.2. Caustic Ingestions
  • Section 4. Stomach and Intestines
  • Chapter 374. Normal Development, Structure, and Function of the Stomach and Intestines
  • DEVELOPMENT
  • DIGESTION AND ABSORPTION
  • THE GASTROINTESTINAL MICROBIOTA
  • Chapter 375. Pyloric Stenosis and Other Congenital Anomalies of the Stomach
  • 375.1. Hypertrophic Pyloric Stenosis
  • 375.2. Congenital Gastric Outlet Obstruction
  • 375.3. Gastric Duplication
  • 375.4. Gastric Volvulus
  • 375.5. Hypertrophic Gastropathy
  • Chapter 376. Intestinal Atresia, Stenosis, and Malrotation
  • 376.1. Duodenal Obstruction
  • 376.2. Jejunal and Ileal Atresia and Obstruction
  • 376.3. Malrotation
  • Chapter 377. Intestinal Duplications, Meckel Diverticulum, and Other Remnants of the Omphalomesenteric Duct
  • 377.1. Intestinal Duplication
  • 377.2. Meckel Diverticulum and Other Remnants of the Omphalomesenteric Duct
  • Chapter 378. Motility Disorders and Hirschsprung Disease
  • 378.1. Chronic Intestinal Pseudoobstruction
  • 378.2. Mitochondrial Neurogastrointestinal Encephalomyopathy
  • 378.3. Encopresis and Functional Constipation
  • 378.4. Congenital Aganglionic Megacolon (Hirschsprung Disease)
  • 378.5. Intestinal Neuronal Dysplasia
  • 378.6. Superior Mesenteric Artery Syndrome (Wilkie Syndrome, Cast Syndrome, Arteriomesenteric Duodenal Compression Syndrome)
  • Chapter 379. Ileus, Adhesions, Intussusception, and Closed-Loop Obstructions
  • 379.1. Ileus
  • 379.2. Adhesions
  • 379.3. Intussusception
  • 379.4. Closed-Loop Obstructions
  • Chapter 380. Foreign Bodies and Bezoars
  • 380.1. Foreign Bodies in the Stomach and Intestine
  • 380.2. Bezoars
  • Chapter 381. Peptic Ulcer Disease in Children
  • PATHOGENESIS
  • 381.1. Zollinger-Ellison Syndrome
  • Chapter 382. Inflammatory Bowel Disease
  • 382.1. Chronic Ulcerative Colitis
  • 382.2. Crohn Disease (Regional Enteritis, Regional Ileitis, Granulomatous Colitis)
  • 382.3. Very Early Onset Inflammatory Bowel Disease
  • Chapter 383. Eosinophilic Gastroenteritis
  • Chapter 384. Celiac Disease
  • ETIOLOGY AND EPIDEMIOLOGY
  • GENETICS AND PATHOGENESIS
  • CLINICAL PRESENTATION AND ASSOCIATED DISORDERS
  • DIAGNOSIS
  • TREATMENT
  • THE SPECTRUM OF GLUTEN-RELATED DISORDERS
  • Chapter 385. Disorders of Malabsorption
  • CLINICAL APPROACH
  • 385.1. Evaluation of Children with Suspected Intestinal Malabsorption
  • 385.2. Other Malabsorptive Syndromes
  • 385.3. Intestinal Infections and Infestations Associated with Malabsorption
  • 385.4. Immunodeficiency Disorders
  • 385.5. Immunoproliferative Small Intestinal Disease
  • 385.6. Short Bowel Syndrome
  • 385.7. Chronic Malnutrition
  • 385.8. Enzyme Deficiencies
  • 385.9. Liver and Biliary Disorders Causing Malabsorption
  • 385.10. Rare Inborn Defects Causing Malabsorption
  • Chapter 386. Intestinal Transplantation in Children with Intestinal Failure
  • INDICATIONS FOR INTESTINAL TRANSPLANT
  • TRANSPLANTATION OPERATION
  • POSTOPERATIVE MANAGEMENT
  • Chapter 387. Acute Gastroenteritis in Children
  • BURDEN OF CHILDHOOD DIARRHEA
  • 387.1. Traveler’s Diarrhea
  • Chapter 388. Chronic Diarrhea
  • PATHOPHYSIOLOGY
  • 388.1. Diarrhea from Neuroendocrine Tumors
  • Chapter 389. Disorders of Brain-Gut Interaction (Functional Gastrointestinal Disorders)
  • DISORDERS OF BRAIN-GUT INTERACTION IN INFANTS AND TODDLERS
  • DISORDERS OF BRAIN-GUT INTERACTION IN OLDER CHILDREN AND ADOLESCENTS
  • DEFECATION DISORDERS
  • Chapter 390. Cyclic Vomiting Syndrome
  • Chapter 391. Acute Appendicitis
  • EPIDEMIOLOGY
  • PATHOPHYSIOLOGY
  • APPENDICITIS RISK SCORING SYSTEMS
  • LABORATORY FINDINGS
  • IMAGING STUDIES
  • DIAGNOSIS AND TREATMENT
  • DIFFERENTIAL DIAGNOSIS
  • ANTIBIOTICS
  • SURGICAL INTERVENTION
  • PERFORATED APPENDICITIS
  • NONOPERATIVE MANAGEMENT OF UNCOMPLICATED APPENDICITIS
  • RECURRENT APPENDICITIS
  • INTERVAL APPENDECTOMY
  • INCIDENTAL APPENDICOLITHS
  • Chapter 392. Surgical Conditions of the Anus and Rectum
  • 392.1. Anorectal Malformations
  • 392.2. Anal Fissure
  • 392.3. Perianal Abscess and Fistula
  • 392.4. Hemorrhoids
  • 392.5. Rectal Mucosal Prolapse
  • Chapter 393. Tumors of the Digestive Tract
  • HAMARTOMATOUS TUMORS
  • ADENOMATOUS TUMORS
  • OTHER GASTROINTESTINAL TUMORS
  • Chapter 394. Inguinal Hernias
  • EMBRYOLOGY AND PATHOGENESIS
  • EVALUATION OF ACUTE INGUINAL-SCROTAL SWELLING
  • DIRECT INGUINAL HERNIA
  • FEMORAL HERNIA
  • COMPLICATIONS
  • Section 5. Exocrine Pancreas
  • Chapter 395. Embryology, Anatomy, and Physiology of the Pancreas
  • Introduction
  • 395.1. Pancreatic Anatomic Abnormalities
  • 395.2. Pancreatic Physiology
  • Chapter 396. Pancreatic Function Tests
  • DIRECT TESTS
  • Chapter 397. Disorders of the Exocrine Pancreas
  • DISORDERS ASSOCIATED WITH PANCREATIC INSUFFICIENCY
  • CYSTIC FIBROSIS
  • SHWACHMAN-DIAMOND SYNDROME
  • PEARSON SYNDROME
  • JOHANSON-BLIZZARD SYNDROME
  • ISOLATED ENZYME DEFICIENCIES
  • OTHER SYNDROMES ASSOCIATED WITH PANCREATIC INSUFFICIENCY
  • Chapter 398. Treatment of Pancreatic Insufficiency
  • Chapter 399. Pancreatitis
  • 399.1Acute Pancreatitis
  • 399.2Acute Recurrent and Chronic Pancreatitis
  • Chapter 400. Pancreatic Fluid Collections
  • TREATMENT OF FLUID COLLECTIONS AND NECROSIS
  • Chapter 401. Pancreatic Tumors
  • Section 6. The Liver and Biliary System
  • Chapter 402. Morphogenesis of the Liver and Biliary System
  • HEPATIC ARCHITECTURE
  • METABOLIC FUNCTIONS OF THE LIVER
  • Chapter 403. Manifestations of Liver Disease
  • PATHOLOGIC MANIFESTATIONS
  • 403.1. Evaluation of Patients with Possible Liver Dysfunction
  • Chapter 404. Cholestasis
  • 404.1. Neonatal Cholestasis
  • 404.2. Cholestasis in the Older Child
  • Chapter 405. Metabolic Diseases of the Liver
  • INTRODUCTION
  • 405.1. Inherited Deficient Conjugation of Bilirubin (Familial Nonhemolytic Unconjugated Hyperbilirubinemia)
  • 405.2. Wilson Disease
  • 405.3. Indian Childhood Cirrhosis
  • 405.4. Neonatal Hemochromatosis
  • 405.5. Miscellaneous Metabolic Diseases of the Liver
  • Chapter 406. Viral Hepatitis
  • ISSUES COMMON TO ALL FORMS OF VIRAL HEPATITIS
  • HEPATITIS A
  • HEPATITIS B
  • HEPATITIS C
  • HEPATITIS D
  • HEPATITIS E
  • APPROACH TO ACUTE OR CHRONIC HEPATITIS
  • Chapter 407. Liver Abscess
  • Chapter 408. Liver Disease Associated with Systemic Disorders
  • INFLAMMATORY BOWEL DISEASE
  • 408.1. Nonalcoholic Fatty Liver Disease
  • Chapter 409. Mitochondrial Hepatopathies
  • EPIDEMIOLOGY
  • CLINICAL MANIFESTATIONS
  • PRIMARY MITOCHONDRIAL HEPATOPATHIES
  • DIAGNOSTIC EVALUATION
  • TREATMENT OF MITOCHONDRIAL HEPATOPATHIES
  • Chapter 410. Autoimmune Hepatitis
  • ETIOLOGY
  • PATHOLOGY
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS
  • DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • Chapter 411. Drug- and Toxin-Induced Liver Injury
  • TREATMENT
  • PROGNOSIS
  • PREVENTION
  • Chapter 412. Acute Hepatic Failure
  • ETIOLOGY
  • PATHOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS
  • TREATMENT
  • PROGNOSIS
  • Chapter 413. Cystic Diseases of the Biliary Tract and Liver
  • CHOLEDOCHAL MALFORMATIONS
  • AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE
  • AUTOSOMAL DOMINANT POLYCYSTIC LIVER DISEASE
  • Chapter 414. Diseases of the Gallbladder
  • ANOMALIES
  • ACUTE HYDROPS
  • CHOLECYSTITIS AND CHOLELITHIASIS
  • BILIARY DYSKINESIA
  • Chapter 415. Portal Hypertension and Varices
  • ETIOLOGY
  • PATHOPHYSIOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • Chapter 416. Liver Transplantation
  • INDICATIONS
  • TECHNICAL INNOVATIONS
  • IMMUNOSUPPRESSION
  • COMPLICATIONS
  • OUTCOMES
  • Section 7. Peritoneum
  • Chapter 417. Peritoneal Malformations
  • Chapter 418. Ascites
  • 418.1. Chylous Ascites
  • Chapter 419. Peritonitis
  • 419.1. Acute Primary Peritonitis
  • 419.2. Acute Secondary Peritonitis
  • 419.3. Acute Secondary Localized Peritonitis (Peritoneal Abscess)
  • Chapter 420. Epigastric Hernia
  • CLINICAL PRESENTATION
  • 420.1. Incisional Hernia
  • The Respiratory System
  • Section 1. Development and Function
  • Chapter 421. Diagnostic Approach to Respiratory Disease
  • HISTORY
  • PHYSICAL EXAMINATION
  • BLOOD GAS ANALYSIS
  • TRANSILLUMINATION OF THE CHEST
  • RADIOGRAPHIC TECHNIQUES
  • PULMONARY FUNCTION TESTING
  • MICROBIOLOGY: EXAMINATION OF LUNG SECRETIONS
  • THE MICROBIOME
  • AIRWAY VISUALIZATION AND LUNG SPECIMEN–BASED DIAGNOSTIC TESTS
  • Chapter 422. Chronic or Recurrent Respiratory Symptoms
  • JUDGING THE SERIOUSNESS OF CHRONIC RESPIRATORY COMPLAINTS
  • 422.1Extrapulmonary Diseases with Pulmonary Manifestations
  • Chapter 423. Sudden Infant Death Syndrome
  • EPIDEMIOLOGY
  • 423.1Sudden Unexpected Postnatal Collapse/Sudden Unexpected Early Neonatal Death
  • Chapter 424. Brief Resolved Unexplained Events and Other Acute Events in Infants
  • DEFINITION
  • EPIDEMIOLOGY
  • INITIAL HISTORY
  • Section 2. Disorders of the Respiratory Tract
  • Chapter 425. Congenital Disorders of the Nose
  • NORMAL NEWBORN NOSE
  • PHYSIOLOGY
  • CONGENITAL DISORDERS
  • CHOANAL ATRESIA
  • CONGENITAL DEFECTS OF THE NASAL SEPTUM
  • PYRIFORM APERTURE STENOSIS
  • CONGENITAL MIDLINE NASAL MASSES
  • DIAGNOSIS AND TREATMENT
  • Chapter 426. Acquired Disorders of the Nose
  • 426.1. Nasal Foreign Bodies
  • 426.2. Epistaxis
  • Chapter 427. Nasal Polyps
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS AND DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • Chapter 428. The Common Cold
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • LABORATORY FINDINGS
  • TREATMENT
  • COMPLICATIONS
  • PREVENTION
  • Chapter 429. Sinusitis
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • COMPLICATIONS
  • PREVENTION
  • Chapter 430. Acute Pharyngitis
  • INFECTIOUS ETIOLOGIES
  • DIAGNOSIS
  • TREATMENT
  • CHRONIC GROUP A STREPTOCOCCUS CARRIERS
  • RECURRENT PHARYNGITIS
  • COMPLICATIONS AND PROGNOSIS
  • PREVENTION
  • Chapter 431. Tonsils and Adenoids
  • NORMAL FUNCTION
  • PATHOLOGY
  • CLINICAL MANIFESTATIONS
  • TREATMENT
  • COMPLICATIONS
  • CHRONIC AIRWAY OBSTRUCTION
  • Chapter 432. Retropharyngeal Abscess, Lateral Pharyngeal (Parapharyngeal) Abscess, and Peritonsillar Cellulitis/Abscess
  • RETROPHARYNGEAL AND LATERAL PHARYNGEAL ABSCESS
  • PERITONSILLAR CELLULITIS AND/OR ABSCESS
  • Chapter 433. Acute Inflammatory Upper Airway Obstruction (Croup, Epiglottitis, Laryngitis, and Bacterial Tracheitis)
  • 433.1. Infectious Upper Airway Obstruction
  • 433.2. Bacterial Tracheitis
  • Chapter 434. Congenital Anomalies of the Larynx, Trachea, and Bronchi
  • Introduction
  • 434.1. Laryngomalacia
  • 434.2. Congenital Subglottic Stenosis
  • 434.3. Vocal Cord Paralysis
  • 434.4. Congenital Laryngeal Webs and Atresia
  • 434.5. Congenital Subglottic Hemangioma
  • 434.6. Laryngoceles and Saccular Cysts
  • 434.7. Posterior Laryngeal Cleft and Laryngotracheoesophageal Cleft
  • 434.8. Vascular and Cardiac Anomalies
  • 434.9. Tracheal Stenoses, Webs, and Atresia
  • 434.10. Foregut Cysts
  • 434.11. Tracheomalacia and Bronchomalacia
  • Chapter 435. Foreign Bodies in the Airway
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • 435.1. Laryngeal Foreign Bodies
  • 435.2. Tracheal Foreign Bodies
  • 435.3. Bronchial Foreign Bodies
  • Chapter 436. Laryngotracheal Stenosis and Subglottic Stenosis
  • 436.1. Congenital Subglottic Stenosis
  • 436.2. Acquired Laryngotracheal Stenosis
  • Chapter 437. Bronchomalacia and Tracheomalacia
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • Chapter 438. Neoplasms of the Larynx, Trachea, and Bronchi
  • 438.1. Vocal Nodules
  • 438.2. Recurrent Respiratory Papillomatosis
  • 438.3. Congenital Subglottic Hemangioma
  • 438.4. Vascular Malformations
  • 438.5. Other Laryngeal Neoplasms
  • 438.6. Tracheal Neoplasms
  • 438.7. Bronchial Tumors
  • Chapter 439. Wheezing, Bronchiolitis, and Bronchitis
  • 439.1. Wheezing in Infants: Bronchiolitis
  • 439.2. Bronchitis
  • Chapter 440. Plastic Bronchitis
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • COMPLICATIONS AND PROGNOSIS
  • Chapter 441. Emphysema and Overinflation
  • LOCALIZED OBSTRUCTIVE OVERINFLATION
  • GENERALIZED OBSTRUCTIVE OVERINFLATION
  • Chapter 442. α1-Antitrypsin Deficiency and Emphysema
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS
  • TREATMENT
  • SUPPORTIVE THERAPY
  • Chapter 443. Other Distal Airway Diseases
  • 443.1. Bronchiolitis Obliterans
  • 443.2. Follicular Bronchitis
  • 443.3. Pulmonary Alveolar Microlithiasis
  • Chapter 444. Congenital Disorders of the Lung
  • 444.1. Pulmonary Agenesis and Aplasia
  • 444.2. Pulmonary Hypoplasia
  • 444.3. Congenital Pulmonary Airway Malformation (Congenital Cystic Adenomatoid Malformation)
  • 444.4. Pulmonary Sequestration
  • 444.5. Bronchogenic Cysts
  • 444.6. Congenital Pulmonary Lymphangiectasia
  • 444.7. Lung Hernia
  • 444.8. Other Congenital Malformations of the Lung
  • Chapter 445. Pulmonary Edema
  • PATHOPHYSIOLOGY
  • ETIOLOGY
  • CLINICAL MANIFESTATIONS
  • TREATMENT
  • Chapter 446. Acute Aspiration
  • ASPIRATION SYNDROMES
  • GASTRIC CONTENTS
  • HYDROCARBON ASPIRATION
  • ASPIRATION OF OTHER SUBSTANCES
  • PRINCIPLES OF MANAGEMENT
  • PREVENTION
  • PROGNOSIS
  • Chapter 447. Chronic Recurrent Aspiration
  • CLINICAL PRESENTATION
  • DIAGNOSIS
  • MANAGEMENT
  • Chapter 448. Immune and Inflammatory Lung Disease
  • 448.1. Hypersensitivity Pneumonia
  • 448.2. Occupational and Environmental Lung Disease
  • 448.3. Granulomatous Lung Disease
  • 448.4. Eosinophilic Lung Disease
  • 448.5. Interstitial Lung Disease
  • 448.6. Neuroendocrine Cell Hyperplasia of Infancy
  • 448.7. Fibrotic Lung Disease
  • Chapter 449. Community-Acquired Pneumonia
  • ETIOLOGY
  • 449.1. COVID-19
  • Chapter 450. E-Cigarette or Vaping Product Use–Associated Lung Injury (EVALI)
  • EPIDEMIOLOGY
  • PATHOPHYSIOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • Chapter 451. Pleurisy, Pleural Effusions, and Empyema
  • 451.1. Dry Pleurisy
  • 451.2. Serofibrinous or Serosanguineous Pleurisy with Pleural Effusion
  • 451.3. Empyema
  • Chapter 452. Bronchiectasis
  • PATHOPHYSIOLOGY AND PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • Chapter 453. Pulmonary Abscess
  • PATHOLOGY AND PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • Chapter 454. Cystic Fibrosis
  • GENETICS
  • PATHOGENESIS
  • PATHOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS AND ASSESSMENT
  • DIAGNOSIS OF CF VIA NEWBORN SCREENING
  • DIAGNOSIS OF CYSTIC FIBROSIS OUTSIDE OF NEWBORN SCREENING
  • OTHER LABORATORY TESTING OF IMPORTANCE IN DIAGNOSIS AND MANAGEMENT
  • MANIFESTATIONS OF REDUCED CFTR FUNCTION THAT DO NOT MEET CRITERIA FOR CF
  • TREATMENT
  • TREATMENT OF PULMONARY COMPLICATIONS
  • TREATMENT OF INTESTINAL COMPLICATIONS
  • OTHER COMPLICATIONS
  • PROGNOSIS
  • Chapter 455. Primary Ciliary Dyskinesia (Immotile Cilia Syndrome, Kartagener Syndrome)
  • NORMAL CILIARY ULTRASTRUCTURE AND FUNCTION
  • GENETICS OF PRIMARY CILIARY DYSKINESIA
  • CLINICAL MANIFESTATIONS OF PRIMARY CILIARY DYSKINESIA
  • DIAGNOSIS OF PRIMARY CILIARY DYSKINESIA
  • TREATMENT
  • PROGNOSIS
  • Chapter 456. Diffuse Lung Diseases in Childhood
  • 456.1. Inherited Disorders of Surfactant Metabolism
  • 456.2. Pulmonary Alveolar Proteinosis
  • Chapter 457. Pulmonary Hemosiderosis
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOLOGY
  • PATHOPHYSIOLOGY
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS AND DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • Chapter 458. Pulmonary Embolism, Infarction, and Hemorrhage
  • 458.1. Pulmonary Embolus and Infarction
  • 458.2. Pulmonary Hemorrhage and Hemoptysis
  • Chapter 459. Atelectasis
  • PATHOPHYSIOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • Chapter 460. Pulmonary Tumors
  • CLINICAL MANIFESTATIONS AND EVALUATION
  • Chapter 461. Pneumothorax
  • ETIOLOGY AND EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS AND DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • Chapter 462. Pneumomediastinum
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS
  • TREATMENT
  • COMPLICATIONS
  • Chapter 463. Hydrothorax
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS
  • TREATMENT
  • Chapter 464. Hemothorax
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • Chapter 465. Chylothorax
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS AND IMAGING
  • TREATMENT
  • COMPLICATIONS
  • Chapter 466. Bronchopulmonary Dysplasia
  • CLINICAL MANIFESTATIONS
  • TREATMENT
  • PROGNOSIS
  • Chapter 467. Skeletal Diseases Influencing Pulmonary Function
  • 467.1. Pectus Excavatum (Funnel Chest)
  • 467.2. Pectus Carinatum and Sternal Clefts
  • 467.3. Asphyxiating Thoracic Dystrophy (Thoracic-Pelvic-Phalangeal Dystrophy)
  • 467.4. Achondroplasia
  • 467.5. Kyphoscoliosis: Adolescent Idiopathic Scoliosis and Congenital Scoliosis
  • 467.6. Congenital Rib Anomalies
  • Chapter 468. Chronic Respiratory Insufficiency
  • 468.1. Chronic Respiratory Failure and Long-Term Mechanical Ventilation
  • 468.2. Congenital Central Hypoventilation Syndrome
  • 468.3. Rapid-Onset Obesity with Hypothalamic Dysfunction, Hypoventilation, and Autonomic Dysregulation
  • 468.4. Long-Term Ventilation and Technology Support: Indications, Principles, Decision-Making, Pragmatics, and Home Provision
  • The Cardiovascular System
  • Section 1. Developmental Biology of the Cardiovascular System
  • Chapter 469. Cardiac Development
  • INTRODUCTION
  • 469.1. Early Cardiac Morphogenesis
  • 469.2. Cardiac Looping
  • 469.3. Cardiac Septation
  • 469.4. Aortic Arch Development
  • 469.5. Cardiac Differentiation
  • 469.6. Developmental Changes in Cardiac Function
  • Chapter 470. The Fetal to Neonatal Circulatory Transition
  • 470.1. The Fetal Circulation
  • 470.2. The Transitional Circulation
  • 470.3. The Neonatal Circulation
  • 470.4. Persistent Pulmonary Hypertension of the Neonate (Persistence of Fetal Circulatory Pathways)
  • Section 2. Evaluation of the Cardiovascular System and the Child With a Heart Murmur
  • Chapter 471. History and Physical Examination in Cardiac Evaluation
  • HISTORY
  • GENERAL PHYSICAL EXAMINATION
  • CARDIAC EXAMINATION
  • Chapter 472. Laboratory Cardiac Evaluation
  • 472.1. Radiologic Cardiac Assessment
  • 472.2. Electrocardiography
  • 472.3. Hematologic Data in Cardiovascular Evaluation
  • 472.4. Echocardiography
  • 472.5. Exercise Testing
  • 472.6. Cardiac Imaging Studies
  • 472.7. Diagnostic and Interventional Cardiac Catheterization
  • Section 3. Congenital Heart Disease
  • Chapter 473. Epidemiology and Genetic Basis of Congenital Heart Disease
  • ETIOLOGY
  • GENETIC COUNSELING
  • Chapter 474. Evaluation and Screening of the Infant or Child with Congenital Heart Disease
  • ACYANOTIC CONGENITAL HEART LESIONS
  • CYANOTIC CONGENITAL HEART LESIONS
  • Chapter 475. Acyanotic Congenital Heart Disease: Left-to-Right Shunt Lesions
  • 475.1. Atrial Septal Defect
  • 475.2. Ostium Secundum Defect
  • 475.3. Sinus Venosus Atrial Septal Defect
  • 475.4. Partial Anomalous Pulmonary Venous Return
  • 475.5. Atrioventricular Septal Defects (Ostium Primum and Atrioventricular Canal or Endocardial Cushion Defects)
  • 475.6. Ventricular Septal Defect
  • 475.7. Supracristal Ventricular Septal Defect with Aortic Insufficiency
  • 475.8. Patent Ductus Arteriosus
  • 475.9. Aortopulmonary Window Defect
  • 475.10. Coronary Artery Fistula
  • 475.11. Ruptured Sinus of Valsalva Aneurysm
  • Chapter 476. Acyanotic Congenital Heart Disease: Obstructive Lesions
  • 476.1. Pulmonary Valve Stenosis with Intact Ventricular Septum
  • 476.2. Infundibular Pulmonary Stenosis and Double-Chamber Right Ventricle
  • 476.3. Pulmonary Stenosis in Combination with an Intracardiac Shunt
  • 476.4. Peripheral Pulmonary Stenosis
  • 476.5. Aortic Stenosis
  • 476.6. Coarctation of the Aorta
  • 476.7. Coarctation with Ventricular Septal Defect
  • 476.8. Coarctation with Other Cardiac Anomalies and Interrupted Aortic Arch
  • 476.9. Congenital Mitral Stenosis
  • 476.10. Pulmonary Venous Hypertension
  • Chapter 477. Acyanotic Congenital Heart Disease: Regurgitant Lesions
  • 477.1. Pulmonary Valvular Insufficiency and Congenital Absence of the Pulmonary Valve
  • 477.2. Congenital Mitral Insufficiency
  • 477.3. Mitral Valve Prolapse
  • 477.4. Tricuspid Regurgitation
  • Chapter 478. Cyanotic Congenital Heart Disease: Evaluation of the Critically Ill Neonate with Cyanosis and Respiratory Distress
  • CARDIAC DISEASE LEADING TO CYANOSIS
  • DIFFERENTIAL DIAGNOSIS
  • Chapter 479. Cyanotic Congenital Heart Disease: Lesions Associated with Decreased Pulmonary Blood Flow
  • 479.1. Tetralogy of Fallot
  • 479.2. Tetralogy of Fallot with Pulmonary Atresia
  • 479.3. Pulmonary Atresia with Intact Ventricular Septum
  • 479.4. Tricuspid Atresia
  • 479.5. Double-Outlet Right Ventricle
  • 479.6. Transposition of the Great Arteries with Ventricular Septal Defect and Pulmonary Stenosis
  • 479.7. Ebstein Anomaly of the Tricuspid Valve
  • Chapter 480. Cyanotic Congenital Heart Disease: Lesions Associated with Increased Pulmonary Blood Flow
  • 480.1. d-Transposition of the Great Arteries
  • 480.2. d-Transposition of the Great Arteries with Intact Ventricular Septum
  • 480.3. Transposition of the Great Arteries with Ventricular Septal Defect
  • 480.4. l-Transposition of the Great Arteries (Corrected Transposition)
  • 480.5. Double-Outlet Right Ventricle Without Pulmonary Stenosis
  • 480.6. Double-Outlet Right Ventricle with Malposition of the Great Arteries (Taussig-Bing Anomaly)
  • 480.7. Total Anomalous Pulmonary Venous Return
  • 480.8. Truncus Arteriosus
  • 480.9. Single Ventricle (Double-Inlet Ventricle, Univentricular Heart)
  • 480.10. Hypoplastic Left Heart Syndrome
  • 480.11. Abnormal Positions of the Heart and the Heterotaxy Syndromes (Asplenia, Polysplenia)
  • Chapter 481. Other Congenital Heart and Vascular Malformations
  • 481.1. Anomalies of the Aortic Arch
  • 481.2. Anomalous Origin of the Coronary Arteries
  • 481.3. Pulmonary Arteriovenous Fistula
  • 481.4. Ectopia Cordis
  • 481.5. Diverticulum of the Left Ventricle
  • Chapter 482. Pulmonary Hypertension
  • 482.1. Primary Pulmonary Hypertension
  • 482.2. Pulmonary Vascular Disease (Eisenmenger Syndrome)
  • Chapter 483. General Principles of Treatment of Congenital Heart Disease
  • POSTOPERATIVE MANAGEMENT
  • 483.1. Congenital Heart Disease in Adults
  • Section 4. Cardiac Arrhythmias
  • Chapter 484. Disturbances of Rate and Rhythm of the Heart
  • 484.1. Principles of Antiarrhythmic Therapy
  • 484.2. Sinus Arrhythmias and Extrasystoles
  • 484.3. Supraventricular Tachycardia
  • 484.4. Ventricular Tachyarrhythmias
  • 484.5. Long QT Syndromes
  • 484.6. Sinus Node Dysfunction
  • 484.7. Atrioventricular Block
  • Chapter 485. Sudden Death
  • MECHANISM OF SUDDEN DEATH
  • CONGENITAL HEART DISEASE
  • CARDIOMYOPATHY
  • CARDIAC ARRHYTHMIA
  • MISCELLANEOUS CAUSES
  • EVALUATION AND THERAPY FOR RESUSCITATED PATIENTS
  • MEDICATION FOR ATTENTION-DEFICIT/HYPERACTIVITY DISORDER
  • PREVENTION OF SUDDEN DEATH
  • Section 5. Acquired Heart Disease
  • Chapter 486. Infective Endocarditis
  • ETIOLOGY
  • EPIDEMIOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • PROGNOSIS AND COMPLICATIONS
  • TREATMENT
  • PREVENTION
  • Chapter 487. Rheumatic Heart Disease
  • PATTERNS OF VALVULAR DISEASE
  • Section 6. Diseases of the Myocardium and Pericardium
  • Chapter 488. Diseases of the Myocardium
  • 488.1. Dilated Cardiomyopathy
  • 488.2. Hypertrophic Cardiomyopathy
  • 488.3. Restrictive Cardiomyopathy
  • 488.4. Left Ventricular Noncompaction, Arrhythmogenic Right Ventricular Cardiomyopathy, Endocardial Fibroelastosis, and Takotsubo Cardiomyopathy
  • 488.5. Myocarditis
  • Chapter 489. Diseases of the Pericardium
  • 489.1. Acute Pericarditis
  • 489.2. Constrictive Pericarditis
  • Chapter 490. Tumors of the Heart
  • Section 7. Cardiac Therapeutics
  • Chapter 491. Heart Failure
  • PATHOPHYSIOLOGY
  • ETIOLOGY OF HEART FAILURE
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • ELECTROPHYSIOLOGIC APPROACHES TO HEART FAILURE MANAGEMENT
  • 491.1. Cardiogenic Shock
  • Chapter 492. Pediatric Heart and Heart-Lung Transplantation
  • 492.1. Pediatric Heart Transplantation
  • 492.2. Heart-Lung and Lung Transplantation
  • Section 8. Diseases of the Peripheral Vascular System
  • Chapter 493. Diseases of the Blood Vessels (Aneurysms and Fistulas)
  • 493.1. Aneurysms
  • 493.2. Arteriovenous Fistulas
  • 493.3. Generalized Arterial Calcification of Infancy (Idiopathic Infantile Arterial Calcification)
  • 493.4. Arterial Tortuosity
  • Chapter 494. Systemic Hypertension
  • PREVALENCE OF HYPERTENSION IN CHILDREN
  • DEFINITION OF HYPERTENSION
  • BLOOD PRESSURE MEASUREMENT IN CHILDREN
  • ETIOLOGY AND PATHOPHYSIOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • PREVENTION
  • TREATMENT
  • Diseases of the Blood
  • Section 1. The Hematopoietic System
  • Chapter 495. Development of the Hematopoietic System
  • HEMATOPOIESIS IN THE HUMAN EMBRYO AND FETUS
  • FETAL GRANULOCYTOPOIESIS
  • FETAL THROMBOPOIESIS
  • FETAL ERYTHROPOIESIS
  • RED CELL LIFE SPAN IN THE FETUS AND NEONATE
  • Chapter 496. Anemias
  • HISTORY AND PHYSICAL EXAMINATION
  • LABORATORY STUDIES
  • DIFFERENTIAL DIAGNOSIS
  • Section 2. Anemias of Inadequate Production
  • Chapter 497. Congenital Hypoplastic Anemia (Diamond-Blackfan Anemia)
  • ETIOLOGY
  • EPIDEMIOLOGY
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS
  • DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • Chapter 498. Pearson Syndrome
  • Chapter 499. Acquired Pure Red Blood Cell Anemia
  • TRANSIENT ERYTHROBLASTOPENIA OF CHILDHOOD
  • RED CELL APLASIA ASSOCIATED WITH PARVOVIRUS B19 INFECTION
  • OTHER RED CELL APLASIAS IN CHILDREN
  • Chapter 500. Anemia of Chronic Disease and Renal Disease
  • 500.1. Anemia of Chronic Disease
  • 500.2. Anemia of Renal Disease
  • Chapter 501. Congenital Dyserythropoietic Anemias
  • CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE I
  • CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE II
  • TRANSCRIPTION FACTOR–RELATED CDA
  • Chapter 502. Physiologic Anemia of Infancy
  • TREATMENT
  • Chapter 503. Megaloblastic Anemias
  • 503.1. Folic Acid Deficiency
  • 503.2. Vitamin B12 (Cobalamin) Deficiency
  • 503.3. Other Rare Megaloblastic Anemias
  • Chapter 504. Iron-Deficiency Anemia
  • ETIOLOGY
  • 504.1. Iron-Refractory Iron-Deficiency Anemia
  • Chapter 505. Other Microcytic Anemias
  • INFANTILE POIKILOCYTOSIS AND HEREDITARY PYROPOIKILOCYTOSIS
  • COPPER DEFICIENCY
  • DEFECTS OF IRON METABOLISM
  • Section 3. Hemolytic Anemias
  • Chapter 506. Definitions and Classification of Hemolytic Anemias
  • Chapter 507. Hereditary Spherocytosis
  • ETIOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • Chapter 508. Hereditary Elliptocytosis, Hereditary Pyropoikilocytosis, and Related Disorders
  • ETIOLOGY
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS
  • TREATMENT
  • Chapter 509. Hereditary Stomatocytosis Syndromes
  • HEREDITARY XEROCYTOSIS
  • HEREDITARY HYDROCYTOSIS
  • INTERMEDIATE SYNDROMES AND OTHER VARIANTS
  • OTHER DISORDERS ASSOCIATED WITH STOMATOCYTOSIS
  • Chapter 510. Paroxysmal Nocturnal Hemoglobinuria and Acanthocytosis
  • PAROXYSMAL NOCTURNAL HEMOGLOBINURIA
  • ACANTHOCYTOSIS
  • Chapter 511. Hemoglobinopathies
  • HEMOGLOBIN DISORDERS
  • 511.1. Sickle Cell Disease
  • 511.2. Sickle Cell Trait (Hemoglobin AS)
  • 511.3. Other Hemoglobinopathies
  • 511.4. Unstable Hemoglobin Disorders
  • 511.5. Abnormal Hemoglobins with Increased Oxygen Affinity
  • 511.6. Abnormal Hemoglobins Causing Cyanosis
  • 511.7. Hereditary Methemoglobinemia
  • 511.8. Hereditary Methemoglobinemia with Deficiency of NADH Cytochrome b5 Reductase
  • 511.9. Syndromes of Hereditary Persistence of Fetal Hemoglobin
  • 511.10. Thalassemia Syndromes
  • Chapter 512. Enzymatic Defects
  • 512.1. Pyruvate Kinase Deficiency
  • 512.2. Other Glycolytic Enzyme Deficiencies
  • 512.3. Glucose-6-Phosphate Dehydrogenase Deficiency and Related Deficiencies
  • Chapter 513. Hemolytic Anemias Resulting from Extracellular Factors—Immune Hemolytic Anemias
  • IMMUNE HEMOLYTIC ANEMIAS
  • AUTOIMMUNE HEMOLYTIC ANEMIAS ASSOCIATED WITH “WARM” ANTIBODIES
  • AUTOIMMUNE HEMOLYTIC ANEMIAS ASSOCIATED WITH “COLD” ANTIBODIES OR COLD AGGLUTININ DISEASE
  • Chapter 514. Hemolytic Anemias Secondary to Other Extracellular Factors
  • FRAGMENTATION HEMOLYSIS
  • THERMAL INJURY
  • RENAL DISEASE
  • LIVER DISEASE
  • TOXINS AND VENOMS
  • WILSON DISEASE
  • Section 4. Polycythemia (Erythrocytosis)
  • Chapter 515. Polycythemia
  • CLONAL POLYCYTHEMIA (POLYCYTHEMIA VERA)
  • Chapter 516. Nonclonal Polycythemia
  • PATHOGENESIS
  • DIAGNOSIS
  • TREATMENT
  • Section 5. The Pancytopenias
  • Chapter 517. Inherited Bone Marrow Failure Syndromes with Pancytopenia
  • FANCONI ANEMIA
  • SHWACHMAN-DIAMOND SYNDROME
  • DYSKERATOSIS CONGENITA
  • CONGENITAL AMEGAKARYOCYTIC THROMBOCYTOPENIA
  • GATA2-RELATED DISORDERS
  • SAMD9/9L-RELATED DISORDER
  • OTHER INHERITED APLASTIC ANEMIAS
  • UNCLASSIFIED INHERITED BONE MARROW FAILURE SYNDROMES
  • Chapter 518. Acquired Pancytopenias
  • ETIOLOGY AND EPIDEMIOLOGY
  • PATHOLOGY AND PATHOGENESIS
  • CLINICAL MANIFESTATIONS, LABORATORY FINDINGS, AND DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • COMPLICATIONS
  • PROGNOSIS
  • PANCYTOPENIA CAUSED BY MARROW REPLACEMENT
  • Section 6. Blood Component Transfusions
  • Chapter 519. Red Blood Cell Transfusions and Erythropoietin Therapy
  • RBC TRANSFUSION IN CHILDREN AND ADOLESCENTS
  • RBC TRANSFUSION IN PRETERM INFANTS AND NEONATES
  • RBC PRODUCT AND DOSE
  • STORAGE AGE OF RBC UNITS
  • Chapter 520. Platelet Transfusions
  • CHILDREN AND ADOLESCENTS
  • INFANTS AND NEONATES
  • PLATELET PRODUCTS AND DOSING
  • Chapter 521. Neutrophil (Granulocyte) Transfusions
  • GRANULOCYTE TRANSFUSIONS FOR CHILDREN
  • GRANULOCYTE TRANSFUSION FOR NEONATES
  • GRANULOCYTE PRODUCT
  • Chapter 522. Plasma Transfusions
  • PLASMA PRODUCTS AND PATIENT TESTING
  • PLASMA TRANSFUSION IN CHILDREN
  • PLASMA TRANSFUSION IN NEONATES
  • Chapter 523. Risks of Blood Transfusions
  • INFECTIOUS RISKS OF TRANSFUSION
  • NONINFECTIOUS RISKS OF TRANSFUSION
  • Section 7. Hemorrhagic and Thrombotic Diseases
  • Chapter 524. Hemostasis
  • THE HEMOSTATIC PROCESS
  • PATHOLOGY
  • 524.1. Clinical and Laboratory Evaluation of Hemostasis
  • Chapter 525. Hereditary Clotting Factor Deficiencies (Bleeding Disorders)
  • 525.1. Factor VIII or Factor IX Deficiency (Hemophilia A or B)
  • 525.2. Factor XI Deficiency
  • 525.3. Deficiencies of the Contact Factors (Nonbleeding Disorders)
  • 525.4. Factor VII Deficiency
  • 525.5. Factor X Deficiency
  • 525.6. Prothrombin (Factor II) Deficiency
  • 525.7. Factor V Deficiency
  • 525.8. Combined Deficiency of Factors V and VIII
  • 525.9. Congenital Fibrinogen Disorders
  • 525.10. Factor XIII Deficiency (Fibrin-Stabilizing Factor or Transglutaminase Deficiency)
  • 525.11. Antiplasmin or Plasminogen Activator Inhibitor Deficiency
  • Chapter 526. Von Willebrand Disease
  • PATHOPHYSIOLOGY
  • CLASSIFICATION
  • LABORATORY DIAGNOSIS
  • TREATMENT
  • Chapter 527. Hereditary Predisposition to Thrombosis
  • Chapter 528. Thrombotic Disorders in Children
  • EPIDEMIOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • LABORATORY TESTING
  • TREATMENT
  • COMPLICATIONS
  • 528.1. Anticoagulant and Thrombolytic Therapy
  • Chapter 529. Postneonatal Vitamin K Deficiency
  • Chapter 530. Coagulopathy in Liver Disease
  • Chapter 531. Acquired Inhibitors of Coagulation
  • LABORATORY FINDINGS
  • TREATMENT
  • Chapter 532. Disseminated Intravascular Coagulation
  • ETIOLOGY
  • LABORATORY FINDINGS
  • CLINICAL MANIFESTATIONS
  • MANAGEMENT
  • Chapter 533. Platelet and Blood Vessel Disorders
  • MEGAKARYOPOIESIS
  • THROMBOCYTOPENIA
  • 533.1. Immune Thrombocytopenia
  • 533.2. Drug-Induced Thrombocytopenia
  • 533.3. Nonimmune Platelet Destruction
  • 533.4. Hemolytic-Uremic Syndrome
  • 533.5. Thrombotic Thrombocytopenic Purpura
  • 533.6. Kasabach-Merritt Syndrome
  • 533.7. Sequestration
  • 533.8. Congenital Thrombocytopenic Syndromes
  • 533.9. Neonatal Thrombocytopenia
  • 533.10. Thrombocytopenia From Acquired Disorders Causing Decreased Production
  • 533.11. Platelet Function Disorders
  • 533.12. Acquired Disorders of Platelet Function
  • 533.13. Congenital Abnormalities of Platelet Function
  • 533.14. Disorders of the Blood Vessels
  • Section 8. The Spleen
  • Chapter 534. Anatomy and Function of the Spleen
  • ANATOMY
  • FUNCTION
  • Chapter 535. Splenomegaly
  • CLINICAL MANIFESTATIONS
  • DIFFERENTIAL DIAGNOSIS
  • Chapter 536. Hyposplenism, Splenic Trauma, and Splenectomy
  • HYPOSPLENISM
  • SPLENIC TRAUMA
  • SPLENECTOMY
  • Section 9. The Lymphatic System
  • Chapter 537. Anatomy and Function of the Lymphatic System
  • Chapter 538. Abnormalities of Lymphatic Vessels
  • LYMPHATIC MALFORMATIONS
  • LYMPHEDEMA
  • LYMPHANGIOLEIOMYOMATOSIS
  • LYMPHANGITIS
  • Chapter 539. Lymphadenopathy
  • DIAGNOSIS
  • 539.1. Kikuchi-Fujimoto Disease (Histiocytic Necrotizing Lymphadenitis)
  • 539.2. Sinus Histiocytosis with Massive Lymphadenopathy (Rosai-Dorfman Disease)
  • 539.3. Castleman Disease (Angiofollicular Lymph Node Hyperplasia)
  • Part XX. Cancer and Benign Tumors
  • Chapter 540. Epidemiology of Childhood and Adolescent Cancer
  • INFLUENCING THE INCIDENCE OF CANCER
  • Chapter 541. Molecular and Cellular Biology of Cancer
  • GENES INVOLVED IN ONCOGENESIS
  • SYNDROMES PREDISPOSING TO CANCER
  • OTHER FACTORS ASSOCIATED WITH ONCOGENESIS
  • Chapter 542. Principles of Cancer Diagnosis
  • SIGNS AND SYMPTOMS
  • PHYSICAL EXAMINATION
  • AGE-RELATED MANIFESTATIONS
  • EARLY DETECTION
  • ENSURING THE DIAGNOSIS
  • STAGING
  • Chapter 543. Principles of Cancer Treatment
  • DIAGNOSIS AND STAGING
  • A MULTIMODAL, MULTIDISCIPLINARY APPROACH
  • DISCUSSING THE TREATMENT PLAN WITH THE PATIENT AND FAMILY
  • TREATMENTS
  • ACUTE TOXIC EFFECTS AND SUPPORTIVE CARE
  • LATE EFFECTS
  • PALLIATIVE CARE
  • Chapter 544. The Leukemias
  • INTRODUCTION
  • 544.1. Acute Lymphoblastic Leukemia
  • 544.2. Acute Myelogenous Leukemia
  • 544.3. Down Syndrome and Acute Leukemia and Transient Abnormal Myelopoiesis
  • 544.4. Chronic Myelogenous Leukemia
  • 544.5. Juvenile Myelomonocytic Leukemia
  • 544.6. Infant Leukemia
  • Chapter 545. Lymphoma
  • INTRODUCTION
  • 545.1. Hodgkin Lymphoma
  • 545.2. Non-Hodgkin Lymphoma
  • 545.3. Late Effects in Children and Adolescents with Lymphoma
  • Chapter 546. Central Nervous System Tumors in Childhood
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • SPECIFIC TUMORS
  • COMPLICATIONS AND LONG-TERM MANAGEMENT
  • Chapter 547. Neuroblastoma
  • EPIDEMIOLOGY
  • PATHOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • Chapter 548. Neoplasms of the Kidney
  • 548.1. Wilms Tumor
  • 548.2. Other Pediatric Renal Tumors
  • Chapter 549. Soft Tissue Sarcomas
  • RHABDOMYOSARCOMA
  • OTHER SOFT TISSUE SARCOMAS
  • Chapter 550. Neoplasms of Bone
  • 550.1. Malignant Tumors of Bone
  • 550.2. Benign Tumors and Tumor-Like Processes of Bone
  • Chapter 551. Retinoblastoma
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • SCREENING
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • Chapter 552. Gonadal and Germ Cell Neoplasms
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS AND DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • Chapter 553. Neoplasms of the Liver
  • HEPATOBLASTOMA
  • HEPATOCELLULAR CARCINOMA
  • Chapter 554. Complex Vascular Anomalies
  • GENETIC BASIS FOR VASCULAR ANOMALIES
  • COMPLEX LYMPHATIC ANOMALIES
  • COMPLEX VENOUS ANOMALIES
  • SYNDROMES ASSOCIATED WITH VASCULAR ANOMALIES
  • CLOVES
  • AKT-RELATED OVERGROWTH SPECTRUM
  • KAPOSIFORM HEMANGIOENDOTHELIOMA
  • OTHER RARE VASCULAR TUMORS
  • LOCALLY AGGRESSIVE RARE VASCULAR TUMORS
  • MALIGNANT TUMORS
  • Chapter 555. Rare Tumors
  • 555.1. Thyroid Tumors
  • 555.2. Nasopharyngeal Carcinoma
  • 555.3. Adenocarcinoma of the Colon and Rectum
  • 555.4. Adrenal Tumors
  • 555.5. Desmoplastic Small Round Cell Tumor
  • Chapter 556. Histiocytosis Syndromes of Childhood
  • INTRODUCTION
  • CLASSIFICATION AND PATHOLOGY
  • 556.1. Langerhans Cell Histiocytosis
  • 556.2. Hemophagocytic Lymphohistiocytosis
  • 556.3. Other Histiocytoses
  • Nephrology
  • Section 1. Glomerular Disease
  • Chapter 557. Introduction to Glomerular Diseases
  • 557.1. Anatomy of the Glomerulus
  • 557.2. Glomerular Filtration
  • 557.3. Glomerular Diseases
  • Section 2. Conditions Particularly Associated With Hematuria
  • Chapter 558. Clinical Evaluation of the Child with Hematuria
  • Chapter 559. Isolated Glomerular Diseases Associated with Recurrent Gross Hematuria
  • Introduction
  • 559.1. Immunoglobulin A Nephropathy (Berger Nephropathy)
  • 559.2. Alport Syndrome
  • 559.3. Thin Basement Membrane Disease
  • 559.4. Acute Poststreptococcal Glomerulonephritis
  • 559.5. Membranous Nephropathy
  • 559.6. Membranoproliferative Glomerulonephritis
  • 559.7. Rapidly Progressive (Crescentic) Glomerulonephritis
  • Chapter 560. Multisystem Disease Associated with Hematuria
  • 560.1. Chronic Infections
  • 560.2. Glomerulonephritis Associated with Systemic Lupus Erythematosus
  • 560.3. IgA Vasculitis Nephritis
  • 560.4. Goodpasture Disease
  • 560.5. Hemolytic-Uremic Syndrome
  • 560.6. Toxic Nephropathy
  • 560.7. Cortical Necrosis
  • 560.8. Coagulopathies and Thrombocytopenia
  • Chapter 561. Tubulointerstitial Disease Associated with Hematuria
  • 561.1. Pyelonephritis
  • 561.2. Tubulointerstitial Nephritis
  • 561.3. Papillary Necrosis
  • 561.4. Acute Tubular Necrosis
  • Chapter 562. Vascular Diseases Associated with Hematuria
  • 562.1. Vascular Abnormalities
  • 562.2. Renal Vein Thrombosis
  • 562.3. Sickle Cell Nephropathy
  • 562.4. Idiopathic Hypercalciuria
  • 562.5. Nephrocalcinosis
  • Chapter 563. Anatomic Abnormalities Associated with Hematuria
  • 563.1. Congenital Anomalies
  • 563.2. Autosomal Recessive Polycystic Kidney Disease
  • 563.3. Autosomal Dominant Polycystic Kidney Disease
  • 563.4. Trauma
  • 563.5. Renal Tumors
  • Chapter 564. Lower Urinary Tract Causes of Hematuria
  • 564.1. Infectious Causes of Cystitis and Urethritis
  • 564.2. Hemorrhagic Cystitis
  • 564.3. Vigorous Exercise
  • Section 3. Conditions Particularly Associated With Proteinuria
  • Chapter 565. Clinical Evaluation of the Child with Proteinuria
  • NORMAL PHYSIOLOGY
  • PATHOPHYSIOLOGY OF PROTEINURIA
  • MEASUREMENT OF URINE PROTEIN
  • CLINICAL CONSIDERATIONS
  • Chapter 566. Conditions Associated with Proteinuria
  • 566.1. Transient Proteinuria
  • 566.2. Orthostatic (Postural) Proteinuria
  • 566.3. Fixed Proteinuria
  • Chapter 567. Nephrotic Syndrome
  • ETIOLOGY
  • 567.1. Idiopathic Nephrotic Syndrome
  • 567.2. Secondary Nephrotic Syndrome
  • 567.3. Congenital Nephrotic Syndrome
  • Section 4. Tubular Disorders
  • Chapter 568. Tubular Function
  • SODIUM
  • POTASSIUM
  • CALCIUM
  • PHOSPHATE
  • MAGNESIUM
  • ACIDIFICATION AND CONCENTRATING MECHANISMS
  • DEVELOPMENTAL CONSIDERATIONS
  • Chapter 569. Renal Tubular Acidosis
  • NORMAL URINARY ACIDIFICATION
  • 569.1. Proximal (Type II) Renal Tubular Acidosis
  • 569.2. Distal (Type I) Renal Tubular Acidosis
  • 569.3. Hyperkalemic (Type IV) Renal Tubular Acidosis
  • 569.4. Rickets Associated with Renal Tubular Acidosis
  • Chapter 570. Nephrogenic Diabetes Insipidus
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT AND PROGNOSIS
  • Chapter 571. Inherited Tubular Transport Abnormalities
  • 571.1. Bartter Syndrome
  • 571.2. Gitelman Syndrome
  • 571.3. Other Inherited Tubular Transport Abnormalities
  • Chapter 572. Renal Failure
  • 572.1. Acute Kidney Injury
  • 572.2. Chronic Kidney Disease
  • 572.3. End-Stage Kidney Disease
  • Chapter 573. Renal Transplantation
  • INCIDENCE AND ETIOLOGY OF ESKD
  • INDICATIONS FOR RENAL TRANSPLANTATION
  • CHARACTERISTICS OF KIDNEY DONORS AND RECIPIENTS
  • EVALUATION AND PREPARING FOR KIDNEY TRANSPLANTATION
  • IMMUNOSUPPRESSION
  • FLUID MANAGEMENT IN INFANTS AND SMALL CHILDREN AFTER KIDNEY TRANSPLANTATION
  • REJECTION OF KIDNEY TRANSPLANT
  • GRAFT SURVIVAL OF KIDNEYS
  • COMPLICATIONS OF IMMUNOSUPPRESSION
  • LONG-TERM OUTCOME OF KIDNEY TRANSPLANTATION
  • Part XXII. Urologic Disorders in Infants and Children
  • Chapter 574. Congenital Anomalies and Dysgenesis of the Kidneys
  • EMBRYONIC AND FETAL DEVELOPMENT
  • RENAL AGENESIS
  • RENAL DYSGENESIS: DYSPLASIA, HYPOPLASIA, AND CYSTIC ANOMALIES
  • RENAL CYSTS IN CHILDREN
  • ANOMALIES IN SHAPE AND POSITION
  • ASSOCIATED PHYSICAL FINDINGS
  • Chapter 575. Urinary Tract Infections
  • PREVALENCE AND ETIOLOGY
  • CLINICAL MANIFESTATIONS AND CLASSIFICATION
  • PATHOGENESIS AND PATHOLOGY
  • DIAGNOSIS
  • IMAGING FINDINGS
  • TREATMENT
  • IMAGING STUDIES IN CHILDREN WITH A FEBRILE UTI
  • PREVENTION OF RECURRENCES
  • Chapter 576. Vesicoureteral Reflux
  • CLASSIFICATION
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • NATURAL HISTORY
  • TREATMENT
  • CURRENT VESICOURETERAL REFLUX GUIDELINES
  • Chapter 577. Obstruction of the Urinary Tract
  • ETIOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • PHYSICAL FINDINGS
  • IMAGING STUDIES
  • SPECIFIC TYPES OF URINARY TRACT OBSTRUCTION AND THEIR TREATMENT
  • Chapter 578. Anomalies of the Bladder
  • BLADDER EXSTROPHY
  • OTHER EXSTROPHY ANOMALIES
  • BLADDER DIVERTICULA
  • URACHAL ANOMALIES
  • Chapter 579. Neuropathic Bladder
  • NEURAL TUBE DEFECTS
  • ASSOCIATED DISORDERS
  • Chapter 580. Enuresis and Voiding Dysfunction
  • NORMAL VOIDING AND TOILET TRAINING
  • DIURNAL INCONTINENCE
  • OVERACTIVE BLADDER (DIURNAL URGE SYNDROME)
  • NONNEUROGENIC NEUROGENIC BLADDER (HINMAN SYNDROME)
  • INFREQUENT VOIDING (UNDERACTIVE BLADDER)
  • VAGINAL VOIDING
  • OTHER CAUSES OF INCONTINENCE IN FEMALES
  • VOIDING DISORDERS WITHOUT INCONTINENCE
  • NOCTURNAL ENURESIS
  • Chapter 581. Anomalies of the Penis and Urethra
  • HYPOSPADIAS
  • CHORDEE WITHOUT HYPOSPADIAS
  • PHIMOSIS AND PARAPHIMOSIS
  • CIRCUMCISION
  • PENILE TORSION
  • INCONSPICUOUS PENIS
  • MICROPENIS
  • PRIAPISM
  • OTHER PENILE ANOMALIES
  • MEATAL STENOSIS
  • OTHER MALE URETHRAL ANOMALIES
  • URETHRAL PROLAPSE (FEMALE)
  • OTHER FEMALE URETHRAL LESIONS
  • Chapter 582. Disorders and Anomalies of the Scrotal Contents
  • UNDESCENDED TESTIS (CRYPTORCHIDISM)
  • SCROTAL SWELLING
  • TESTICULAR (SPERMATIC CORD) TORSION
  • TORSION OF THE APPENDIX TESTIS/EPIDIDYMIS
  • EPIDIDYMITIS
  • VARICOCELE
  • SPERMATOCELE
  • HYDROCELE
  • INGUINAL HERNIA
  • TESTICULAR MICROLITHIASIS
  • TESTICULAR TUMOR
  • Chapter 583. Trauma to the Genitourinary Tract
  • DIAGNOSIS
  • TREATMENT
  • Chapter 584. Urinary Lithiasis
  • STONE FORMATION
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • METABOLIC EVALUATION
  • PATHOGENESIS OF SPECIFIC RENAL CALCULI
  • TREATMENT
  • STONE PREVENTION
  • Part XXIII. Gynecologic Problems of Childhood
  • Chapter 585. Gynecologic History and Physical Examination
  • HISTORY
  • GYNECOLOGIC EXAMINATION
  • Chapter 586. Vulvovaginitis
  • ETIOLOGY
  • EPIDEMIOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS AND DIFFERENTIAL DIAGNOSIS
  • TREATMENT AND PREVENTION
  • Chapter 587. Vaginal Bleeding in the Prepubertal Child
  • Chapter 588. Breast Health
  • BREAST DEVELOPMENT
  • BREAST EXAMINATION
  • BREAST SELF-AWARENESS
  • ABNORMAL DEVELOPMENT
  • BREAST MASSES
  • MANAGEMENT OF BREAST MASSES
  • Chapter 589. Polycystic Ovary Syndrome and Hirsutism
  • POLYCYSTIC OVARY SYNDROME
  • HIRSUTISM
  • Chapter 590. Gynecologic Neoplasms and Prevention Methods for Human Papillomavirus Infections in Adolescents
  • OVERVIEW OF GYNECOLOGIC MALIGNANCIES IN CHILDREN AND ADOLESCENTS
  • IMPACT OF CANCER THERAPY ON FERTILITY
  • NEONATAL AND PEDIATRIC OVARIAN CYSTS
  • OVARIAN NEOPLASMS
  • OVARIAN MALIGNANCIES
  • UTERINE MALIGNANCIES
  • VAGINAL MALIGNANCIES
  • VULVAR MALIGNANCIES
  • CERVICAL MALIGNANCIES AND THEIR PREVENTION
  • Chapter 591. Vulvovaginal and Müllerian Anomalies
  • EMBRYOLOGY
  • EPIDEMIOLOGY
  • CLINICAL MANIFESTATIONS
  • LABORATORY AND RADIOGRAPHIC FINDINGS
  • UTERINE ANOMALIES
  • VAGINAL ANOMALIES
  • CERVICAL ANOMALIES
  • VULVAR AND OTHER ANOMALIES
  • Chapter 592. Gynecologic Care for Adolescents with Special Needs
  • SEXUALITY AND SEXUAL EDUCATION
  • ABUSE
  • PELVIC EXAMINATION
  • MENSTRUATION
  • CONTRACEPTION
  • Chapter 593. Female Genital Mutilation
  • COMPLICATIONS
  • CLINICAL MANAGEMENT OF FGM
  • The Endocrine System
  • Section 1. Disorders of the Hypothalamus and Pituitary Gland
  • Chapter 594. Hormones of the Hypothalamus and Pituitary
  • ANATOMY
  • EMBRYOLOGY
  • VASCULAR SUPPLY
  • ANTERIOR PITUITARY CELL TYPES
  • POSTERIOR PITUITARY CELL TYPES
  • Chapter 595. Hypopituitarism
  • MULTIPLE PITUITARY HORMONE DEFICIENCY
  • ISOLATED GROWTH HORMONE DEFICIENCY AND INSENSITIVITY
  • GROWTH HORMONE INSENSITIVITY
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS
  • RADIOLOGIC FINDINGS
  • DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • COMPLICATIONS AND ADVERSE EFFECTS OF GROWTH HORMONE TREATMENT
  • Chapter 596. Diabetes Insipidus
  • PHYSIOLOGY OF WATER BALANCE
  • APPROACH TO THE PATIENT WITH POLYURIA, POLYDIPSIA, AND HYPERNATREMIA
  • CAUSES OF HYPERNATREMIA
  • TREATMENT OF CENTRAL DIABETES INSIPIDUS
  • TREATMENT OF NEPHROGENIC DIABETES INSIPIDUS
  • Chapter 597. Other Abnormalities of Arginine Vasopressin Metabolism and Action
  • CAUSES OF HYPONATREMIA
  • TREATMENT
  • Chapter 598. Hyperpituitarism
  • SECONDARY HYPERPITUITARISM
  • EXCESS GROWTH HORMONE SECRETION AND PITUITARY GIGANTISM
  • TREATMENT OF NORMAL-VARIANT TALL STATURE
  • HYPERSECRETION OF OTHER PITUITARY HORMONES
  • 598.1. Overgrowth Syndromes
  • Chapter 599. Physiology of Puberty
  • Chapter 600. Disorders of Pubertal Development
  • INTRODUCTION
  • 600.1. Central Precocious Puberty
  • 600.2. Precocious Puberty Resulting from Organic Brain Lesions
  • 600.3. Precocious Puberty After Irradiation of the Brain
  • 600.4. Syndrome of Precocious Puberty and Hypothyroidism
  • 600.5. Chorionic Gonadotropin-Secreting Tumors: Paraneoplastic Precocious Puberty
  • 600.6. McCune-Albright Syndrome
  • 600.7. Familial Male-Limited Gonadotropin-Independent Precocious Puberty
  • 600.8. Incomplete (Partial) Precocious Development
  • 600.9. Medicational Precocity
  • 600.10. Delayed or Absent Puberty
  • Section 2. Disorders of the Thyroid Gland
  • Chapter 601. Thyroid Development and Physiology
  • FETAL DEVELOPMENT
  • 601.1. Thyroid Hormone Studies
  • Chapter 602. Disorders of Thyroxine-Binding Globulin
  • Chapter 603. Hypothyroidism
  • CONGENITAL HYPOTHYROIDISM
  • ACQUIRED HYPOTHYROIDISM
  • Chapter 604. Thyroiditis
  • THYROIDITIS WITH PAIN
  • THYROIDITIS WITHOUT PAIN
  • OTHER CAUSES OF THYROIDITIS
  • Chapter 605. Goiter
  • 605.1. Congenital Goiter
  • 605.2. Intratracheal Goiter
  • 605.3. Endemic Goiter and Cretinism
  • 605.4. Acquired Goiter
  • Chapter 606. Thyrotoxicosis
  • 606.1. Graves Disease
  • 606.2. Congenital Hyperthyroidism
  • Chapter 607. Carcinoma of the Thyroid
  • PATHOGENESIS
  • 607.1. Thyroid Nodules
  • Chapter 608. Autoimmune Polyglandular Syndromes
  • MONOGENIC AUTOIMMUNE POLYGLANDULAR SYNDROMES
  • AUTOIMMUNE POLYGLANDULAR SYNDROME TYPE 1
  • IMMUNE DYSREGULATION-POLYENDOCRINOPATHY-ENTEROPATHY X-LINKED
  • OTHER MONOGENIC IMMUNE DYSREGULATION DISORDERS
  • POLYGENIC AUTOIMMUNE POLYGLANDULAR SYNDROME
  • CHROMOSOMAL ABNORMALITIES ASSOCIATED WITH AUTOIMMUNE POLYGLANDULAR SYNDROME
  • NONGENETIC AUTOIMMUNE CAUSES OF MULTIPLE ENDOCRINOPATHY
  • Chapter 609. Multiple Endocrine Neoplasia Syndromes
  • MULTIPLE ENDOCRINE NEOPLASIA TYPE 1
  • MULTIPLE ENDOCRINE NEOPLASIA TYPE 2
  • MULTIPLE ENDOCRINE NEOPLASIA TYPE 2A
  • MULTIPLE ENDOCRINE NEOPLASIA TYPE 2B
  • FAMILIAL MEDULLARY THYROID CARCINOMA
  • MANAGEMENT OF MULTIPLE ENDOCRINE NEOPLASIA TYPE 2
  • Section 3. Disorders of the Parathyroid Gland
  • Chapter 610. Hormones and Peptides of Calcium Homeostasis and Bone Metabolism
  • PARATHYROID HORMONE
  • PARATHYROID HORMONE–RELATED PEPTIDE
  • VITAMIN D
  • CALCITONIN
  • Chapter 611. Hypoparathyroidism
  • APLASIA OR HYPOPLASIA OF THE PARATHYROID GLANDS
  • X-LINKED RECESSIVE HYPOPARATHYROIDISM
  • AUTOSOMAL RECESSIVE HYPOPARATHYROIDISM WITH DYSMORPHIC FEATURES
  • HYPOPARATHYROIDISM, SENSORINEURAL DEAFNESS, AND RENAL ANOMALY SYNDROME
  • SUPPRESSION OF NEONATAL PARATHYROID HORMONE SECRETION BECAUSE OF MATERNAL HYPERPARATHYROIDISM OR MATERNAL FAMILIAL HYPOCALCIURIC HYPERCALCEMIA
  • AUTOSOMAL DOMINANT HYPOPARATHYROIDISM
  • HYPOPARATHYROIDISM ASSOCIATED WITH MITOCHONDRIAL DISORDERS
  • SURGICAL OR INFILTRATIVE HYPOPARATHYROIDISM
  • AUTOIMMUNE HYPOPARATHYROIDISM
  • IDIOPATHIC HYPOPARATHYROIDISM
  • Chapter 612. Pseudohypoparathyroidism
  • TYPE Ia
  • TYPE Ib
  • ACRODYSOSTOSIS WITH HORMONE RESISTANCE
  • Chapter 613. Hyperparathyroidism
  • ETIOLOGY
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS
  • DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • 613.1. Other Causes of Hypercalcemia
  • Section 4. Disorders of the Adrenal Gland
  • Chapter 614. Physiology of the Adrenal Gland
  • 614.1. Histology and Embryology
  • 614.2. Adrenal Steroid Biosynthesis
  • 614.3. Regulation of the Adrenal Cortex
  • 614.4. Adrenal Steroid Hormone Actions
  • 614.5. Adrenal Medulla
  • Chapter 615. Adrenocortical Insufficiency and Altered Sensitivity to Corticosteroids
  • 615.1. Primary Adrenal Insufficiency
  • 615.2. Secondary and Tertiary Adrenal Insufficiency
  • 615.3. Adrenal Insufficiency in the Critical Care Setting
  • 615.4. Altered End-Organ Sensitivity to Corticosteroids
  • Chapter 616. Congenital Adrenal Hyperplasia and Related Disorders
  • 616.1. Congenital Adrenal Hyperplasia Caused by 21-Hydroxylase Deficiency
  • 616.2. Congenital Adrenal Hyperplasia Caused by 11β-Hydroxylase Deficiency
  • 616.3. Congenital Adrenal Hyperplasia Caused by 3β-Hydroxysteroid Dehydrogenase Deficiency
  • 616.4. Congenital Adrenal Hyperplasia Caused by 17-Hydroxylase Deficiency
  • 616.5. Lipoid Adrenal Hyperplasia
  • 616.6. Deficiency of P450 Oxidoreductase (Antley-Bixler Syndrome)
  • 616.7. Aldosterone Synthase Deficiency
  • 616.8. Glucocorticoid-Remediable Aldosteronism
  • Chapter 617. Adrenocortical Tumors and Masses
  • 617.1. Adrenocortical Carcinoma
  • 617.2. Adrenal Incidentaloma
  • 617.3. Adrenal Calcification
  • Chapter 618. Virilizing and Feminizing Adrenal Tumors
  • LABORATORY FINDINGS
  • DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • Chapter 619. Cushing Syndrome
  • ETIOLOGY
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS
  • DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • Chapter 620. Primary Aldosteronism
  • EPIDEMIOLOGY
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS
  • DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • Chapter 621. Pheochromocytoma
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS
  • DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • Section 5. Disorders of the Gonads
  • Chapter 622. Development and Function of the Gonads
  • GENETIC CONTROL OF EMBRYONIC GONADAL DIFFERENTIATION
  • FUNCTION OF THE TESTES
  • FUNCTION OF THE OVARIES
  • DIAGNOSTIC TESTING
  • Chapter 623. Hypofunction of the Testes
  • 623.1. Hypergonadotropic Hypogonadism in the Male (Primary Hypogonadism)
  • 623.2. Hypogonadotropic Hypogonadism in the Male (Secondary Hypogonadism)
  • Chapter 624. Pseudoprecocity Resulting from Tumors of the Testes
  • Chapter 625. Gynecomastia
  • PHYSIOLOGIC FORMS OF GYNECOMASTIA
  • EVALUATION OF GYNECOMASTIA
  • TREATMENT
  • Chapter 626. Hypofunction of the Ovaries
  • 626.1. Hypergonadotropic Hypogonadism in the Female (Primary Hypogonadism)
  • 626.2. Hypogonadotropic Hypogonadism in the Female (Secondary Hypogonadism)
  • Chapter 627. Pseudoprecocity Resulting from Lesions of the Ovary
  • ESTROGENIC LESIONS OF THE OVARY
  • ANDROGENIC LESIONS OF THE OVARY
  • Chapter 628. Disorders of Sex Development
  • SEX DIFFERENTIATION
  • 628.1. 46,XX DSD
  • 628.2. 46,XY DSD
  • 628.3. Ovotesticular DSD
  • Section 6. Diabetes Mellitus in Children
  • Chapter 629. Diabetes Mellitus
  • 629.1. Classification of Diabetes Mellitus
  • 629.2. Type 1 Diabetes Mellitus (Immune Mediated)
  • 629.3. Type 2 Diabetes Mellitus
  • 629.4. Other Specific Types of Diabetes
  • Part XXV. The Nervous System
  • Chapter 630. Neurologic Evaluation
  • HISTORY
  • NEUROLOGIC EXAMINATION
  • GENERAL EXAMINATION
  • SPECIAL DIAGNOSTIC PROCEDURES
  • Chapter 631. Congenital Anomalies of the Central Nervous System
  • 631.1. Neural Tube Defects
  • 631.2. Myelomeningocele
  • 631.3. Occult Spinal Dysraphism
  • 631.4. Encephalocele
  • 631.5. Anencephaly
  • 631.6. Malformations of Cortical Development
  • 631.7. Disorders with Midline Defects
  • 631.8. Dysgenesis of the Cranial Nerves and the Posterior Fossa
  • 631.9. Hydrocephalus
  • 631.10. Craniosynostosis
  • Chapter 632. Deformational Plagiocephaly
  • EPIDEMIOLOGY AND ETIOLOGY
  • EXAMINATION AND DIFFERENTIATING BETWEEN DEFORMATIONAL PLAGIOCEPHALY AND CRANIOSYNOSTOSIS
  • TREATMENT
  • OUTCOMES
  • Chapter 633. Seizures in Childhood
  • EVALUATION OF THE FIRST SEIZURE
  • 633.1. Febrile Seizures
  • 633.2. Unprovoked Seizures
  • 633.3. Focal Seizures and Related Epilepsy Syndromes
  • 633.4. Generalized Seizures and Related Epilepsy Syndromes
  • 633.5. Mechanisms of Seizures
  • 633.6. Treatment of Seizures and Epilepsy
  • 633.7. Neonatal Seizures
  • 633.8. Status Epilepticus
  • 633.9. Reflex Seizures (Stimulus-Precipitated Seizures)
  • 633.10. Nodding Syndrome
  • Chapter 634. Conditions That Mimic Seizures
  • SYNCOPE AND OTHER GENERALIZED PAROXYSMS
  • MOVEMENT DISORDERS AND OTHER PAROXYSMAL MOVEMENTS AND POSTURES
  • OCULOMOTOR AND VISUAL ABNORMALITIES
  • SLEEP-RELATED DISORDERS (see also Chapter 31)
  • Chapter 635. Headaches
  • 635.1. Migraine
  • 635.2. Secondary Headaches
  • 635.3. Tension-Type Headaches
  • Chapter 636. Neurocutaneous Syndromes
  • 636.1. Neurofibromatosis
  • 636.2. Tuberous Sclerosis
  • 636.3. Sturge-Weber Syndrome
  • 636.4. Von Hippel-Lindau Disease
  • 636.5. Linear Nevus Sebaceous Syndrome
  • 636.6. PHACE Syndrome
  • 636.7. Incontinentia Pigmenti
  • Chapter 637. Movement Disorders
  • Introduction
  • 637.1. Ataxias
  • 637.2. Chorea, Athetosis, and Tremor
  • 637.3. Myoclonus
  • 637.4. Dystonia
  • Chapter 638. Encephalopathies
  • 638.1. Cerebral Palsy
  • 638.2. Mitochondrial Encephalomyopathies
  • 638.3. Other Encephalopathies
  • 638.4. Autoimmune Encephalitis
  • Chapter 639. Neurodegenerative Disorders of Childhood
  • 639.1. Sphingolipidoses
  • 639.2. Neuronal Ceroid Lipofuscinoses
  • 639.3. Adrenoleukodystrophy
  • 639.4. Sialidosis
  • 639.5. Miscellaneous Neurodegenerative Disorders
  • Chapter 640. Demyelinating Disorders of the Central Nervous System
  • Introduction
  • 640.1. Acute Disseminated Encephalomyelitis
  • 640.2. Optic Neuritis
  • 640.3. Transverse Myelitis
  • 640.4. Multiple Sclerosis
  • 640.5. Myelin Oligodendrocyte Glycoprotein–Associated Disorders
  • 640.6. Neuromyelitis Optica Spectrum Disorders
  • Chapter 641. Pediatric Stroke
  • 641.1. Arterial Ischemic Stroke
  • 641.2. Cerebral Sinovenous Thrombosis
  • 641.3. Spinal Cord Lesions Associated with Vascular Processes
  • 641.4. Hemorrhagic Stroke
  • 641.5. Differential Diagnosis of Strokelike Events
  • Chapter 642. Central Nervous System Vasculitis
  • EPIDEMIOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • Chapter 643. Central Nervous System Infections
  • 643.1. Acute Bacterial Meningitis Beyond the Neonatal Period
  • 643.2. Viral Meningoencephalitis
  • 643.3. Eosinophilic Meningitis
  • Chapter 644. Brain Abscess
  • PATHOLOGY
  • ETIOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • Chapter 645. Idiopathic Intracranial Hypertension (Pseudotumor Cerebri)
  • ETIOLOGY
  • CLINICAL MANIFESTATIONS
  • TREATMENT
  • Chapter 646. Spinal Cord Disorders
  • 646.1. Tethered Cord
  • 646.2. Diastematomyelia (Split-Cord Malformation)
  • 646.3. Syringomyelia
  • 646.4. Spinal Cord Tumors
  • 646.5. Spinal Arteriovenous Malformations
  • Part XXVI. Neuromuscular Disorders
  • Chapter 647. Evaluation and Investigation of Neuromuscular Disorders
  • GENETIC TESTING
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS
  • IMAGING OF MUSCLES AND THE CENTRAL NERVOUS SYSTEM
  • MUSCLE BIOPSY
  • NERVE BIOPSY
  • CARDIAC ASSESSMENT
  • Chapter 648. Developmental Disorders of Muscle
  • MYOGENIC REGULATORY GENES AND GENETIC LOCI OF INHERITED DISEASES OF MUSCLE
  • 648.1. Myotubular Myopathy (Centronuclear Myopathy)
  • 648.2. Congenital Muscle Fiber–Type Disproportion
  • 648.3. Nemaline Rod Myopathy
  • 648.4. Core Myopathies
  • 648.5. Myofibrillar Myopathies
  • 648.6. Brain Malformations and Muscle Development
  • 648.7. Amyoplasia
  • 648.8. Muscular Dysgenesis (Proteus Syndrome Myopathy)
  • 648.9. Benign Congenital Hypotonia
  • 648.10. Arthrogryposis
  • Chapter 649. Muscular Dystrophies
  • 649.1. Duchenne and Becker Muscular Dystrophies
  • 649.2. Emery-Dreifuss Muscular Dystrophy/Laminopathies
  • 649.3. Myotonic Muscular Dystrophy
  • 649.4. Limb-Girdle Muscular Dystrophies
  • 649.5. Facioscapulohumeral Muscular Dystrophy
  • 649.6. Congenital Muscular Dystrophies
  • Chapter 650. Endocrine and Toxic Myopathies
  • THYROID MYOPATHIES
  • STEROID-HORMONE INDUCED MYOPATHY
  • STATIN-INDUCED RHABDOMYOLYSIS WITH MYOGLOBINURIA
  • MITOCHONDRIAL DYSFUNCTION IN TOXIC MYOPATHIES
  • CRITICAL ILLNESS MYOPATHY
  • Chapter 651. Metabolic Myopathies and Channelopathies
  • 651.1. Periodic Paralyses and Other Muscle Channelopathies
  • 651.2. Malignant Hyperthermia
  • 651.3. Glycogenoses
  • 651.4. Mitochondrial Myopathies
  • 651.5. Lipid Myopathies
  • 651.6. Vitamin E Deficiency Myopathy
  • Chapter 652. Disorders of Neuromuscular Transmission and of Motor Neurons
  • 652.1. Myasthenia Gravis
  • 652.2. Spinal Muscular Atrophies
  • 652.3. Other Motor Neuron Diseases
  • Chapter 653. Hereditary Motor-Sensory Neuropathies
  • Introduction
  • 653.1. Peroneal Muscular Atrophy (Charcot-Marie-Tooth Disease, HMSN Type IIa)
  • 653.2. Peroneal Muscular Atrophy (Axonal Type)
  • 653.3. Congenital Hypomyelinating Neuropathy and Déjèrine-Sottas Disease (HMSN Type III)
  • 653.4. Roussy-Lévy Syndrome
  • 653.5. Refsum Disease (HMSN Type IV) and Infantile Refsum Disease
  • 653.6. Fabry Disease
  • 653.7. Giant Axonal Neuropathy
  • 653.8. Hypermyelinating (Tomaculous) Neuropathy; Hereditary Neuropathy with Liability to Pressure Palsies
  • 653.9. Leukodystrophies
  • 653.10. Congenital Hereditary Sensory Pain Syndromes
  • Chapter 654. Toxic Neuropathies
  • Chapter 655. Autonomic Neuropathies
  • 655.1. Familial Dysautonomia
  • 655.2. Other Autonomic Neuropathies
  • Chapter 656. Guillain-Barré Syndrome
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS AND DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • Chapter 657. Bell Palsy
  • CLINICAL MANIFESTATIONS
  • TREATMENT
  • PROGNOSIS
  • FACIAL PALSY AT BIRTH
  • Part XXVII. Disorders of the Eye
  • Chapter 658. Growth and Development of the Eye
  • Chapter 659. Examination of the Eye
  • VISUAL ACUITY
  • VISUAL FIELD ASSESSMENT
  • COLOR VISION TESTING
  • PUPILLARY EXAMINATION
  • OCULAR MOTILITY
  • BINOCULAR VISION
  • EXTERNAL EXAMINATION
  • BIOMICROSCOPY (SLIT-LAMP EXAMINATION)
  • FUNDUS EXAMINATION (OPHTHALMOSCOPY)
  • REFRACTION
  • TONOMETRY
  • Chapter 660. Abnormalities of Refraction and Accommodation
  • HYPEROPIA
  • MYOPIA
  • ASTIGMATISM
  • ANISOMETROPIA
  • ACCOMMODATION
  • Chapter 661. Disorders of Vision
  • AMBLYOPIA
  • DIPLOPIA
  • SUPPRESSION
  • AMAUROSIS
  • NYCTALOPIA
  • PSYCHOGENIC DISTURBANCES
  • DYSLEXIA
  • Chapter 662. Abnormalities of Pupil and Iris
  • ANIRIDIA
  • COLOBOMA OF THE IRIS
  • MICROCORIA
  • CONGENITAL MYDRIASIS
  • DYSCORIA AND CORECTOPIA
  • ANISOCORIA
  • DILATED FIXED PUPIL
  • TONIC PUPIL
  • MARCUS GUNN PUPIL
  • HORNER SYNDROME
  • PARADOXICAL PUPIL REACTION
  • PERSISTENT PUPILLARY MEMBRANE
  • HETEROCHROMIA
  • OTHER IRIS LESIONS
  • LEUKOCORIA
  • Chapter 663. Disorders of Eye Movement and Alignment
  • STRABISMUS
  • CONGENITAL OCULAR MOTOR APRAXIA
  • NYSTAGMUS
  • OTHER ABNORMAL EYE MOVEMENTS
  • Chapter 664. Abnormalities of the Lids
  • PTOSIS
  • EPICANTHAL FOLDS
  • LAGOPHTHALMOS
  • LID RETRACTION
  • ECTROPION, ENTROPION, AND EPIBLEPHARON
  • BLEPHAROSPASM
  • BLEPHARITIS
  • HORDEOLUM (STYE)
  • CHALAZION
  • COLOBOMA OF THE EYELID
  • TUMORS OF THE LID
  • Chapter 665. Disorders of the Lacrimal System
  • THE TEAR FILM
  • DACRYOSTENOSIS
  • ALACRIMA AND “DRY EYE”
  • Chapter 666. Disorders of the Conjunctiva
  • CONJUNCTIVITIS
  • OTHER CONJUNCTIVAL DISORDERS
  • Chapter 667. Abnormalities of the Cornea
  • MEGALOCORNEA
  • MICROCORNEA
  • KERATOCONUS
  • NEONATAL CORNEAL OPACITIES
  • SCLEROCORNEA
  • PETERS ANOMALY
  • CORNEAL DYSTROPHIES
  • DERMOIDS
  • DENDRITIC KERATITIS
  • CORNEAL ULCERS
  • PHLYCTENULES
  • INTERSTITIAL KERATITIS
  • CORNEAL MANIFESTATIONS OF SYSTEMIC DISEASE
  • Chapter 668. Abnormalities of the Lens
  • CATARACTS
  • ECTOPIA LENTIS
  • OTHER DISORDERS OF THE LENS
  • Chapter 669. Disorders of the Uveal Tract
  • UVEITIS (IRITIS, CYCLITIS, CHORIORETINITIS)
  • Chapter 670. Disorders of the Retina and Vitreous
  • RETINOPATHY OF PREMATURITY
  • PERSISTENT FETAL VASCULATURE
  • RETINOBLASTOMA
  • INHERITED RETINAL DYSTROPHIES
  • STARGARDT DISEASE (FUNDUS FLAVIMACULATUS)
  • BEST VITELLIFORM DEGENERATION
  • CHERRY-RED SPOT
  • PHAKOMATOSIS
  • RETINOSCHISIS
  • RETINAL DETACHMENT
  • COATS DISEASE
  • FAMILIAL EXUDATIVE VITREORETINOPATHY
  • HYPERTENSIVE RETINOPATHY
  • DIABETIC RETINOPATHY
  • SUBACUTE BACTERIAL ENDOCARDITIS
  • BLOOD DISORDERS
  • TRAUMA-RELATED RETINOPATHY
  • MYELINATED NERVE FIBERS
  • CHORIORETINAL COLOBOMA
  • Chapter 671. Abnormalities of the Optic Nerve
  • OPTIC NERVE APLASIA
  • OPTIC NERVE HYPOPLASIA
  • OPTIC NERVE COLOBOMA
  • MORNING GLORY DISC ANOMALY
  • TILTED DISC
  • DRUSEN OF THE OPTIC NERVE
  • PAPILLEDEMA
  • OPTIC NEURITIS
  • LEBER HEREDITARY OPTIC NEUROPATHY
  • OPTIC ATROPHY
  • OPTIC NERVE GLIOMA
  • TRAUMATIC OPTIC NEUROPATHIES
  • Chapter 672. Childhood Glaucoma
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS AND TREATMENT
  • Chapter 673. Orbital Abnormalities
  • HYPERTELORISM AND HYPOTELORISM
  • EXOPHTHALMOS AND ENOPHTHALMOS
  • ORBITAL INFLAMMATION
  • TUMORS OF THE ORBIT
  • Chapter 674. Orbital Infections
  • DACRYOADENITIS
  • DACRYOCYSTITIS
  • PRESEPTAL CELLULITIS
  • ORBITAL CELLULITIS
  • ENDOPHTHALMITIS
  • Chapter 675. Injuries to the Eye
  • ECCHYMOSIS AND SWELLING OF THE EYELIDS
  • LACERATIONS OF THE EYELIDS
  • SUPERFICIAL ABRASIONS OF THE CORNEA
  • FOREIGN BODY INVOLVING THE OCULAR SURFACE
  • HYPHEMA
  • OPEN GLOBE
  • OPTIC NERVE TRAUMA
  • CHEMICAL INJURIES
  • ORBITAL FRACTURES
  • PENETRATING WOUNDS OF THE ORBIT
  • CHILD ABUSE
  • FIREWORKS-RELATED INJURIES
  • SPORTS-RELATED OCULAR INJURIES AND THEIR PREVENTION
  • HANDHELD LASER RETINAL INJURY
  • Part XXVIII. The Ear
  • Chapter 676. General Considerations and Evaluation of the Ear
  • CLINICAL MANIFESTATIONS
  • FACIAL PARALYSIS
  • PHYSICAL EXAMINATION
  • Chapter 677. Hearing Loss
  • INCIDENCE AND PREVALENCE
  • TYPES OF HEARING LOSS
  • ETIOLOGY
  • EFFECTS OF HEARING IMPAIRMENT
  • HEARING SCREENING
  • IDENTIFICATION OF HEARING IMPAIRMENT
  • CLINICAL AUDIOLOGIC EVALUATION
  • TREATMENT
  • GENETIC COUNSELING
  • 677.1. Idiopathic Sudden Sensorineural Hearing Loss
  • Chapter 678. Congenital Malformations of the Ear
  • PINNA MALFORMATIONS
  • CONGENITAL STENOSIS OR ATRESIA OF THE EXTERNAL AUDITORY CANAL
  • CONGENITAL MIDDLE-EAR MALFORMATIONS
  • CONGENITAL INNER EAR MALFORMATIONS
  • CONGENITAL CHOLESTEATOMA
  • Chapter 679. External Otitis (Otitis Externa)
  • ETIOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • TREATMENT
  • PREVENTION
  • OTHER DISEASES OF THE EXTERNAL EAR
  • Chapter 680. Otitis Media
  • EPIDEMIOLOGY
  • ETIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • EXAMINATION OF THE TYMPANIC MEMBRANE
  • PREVENTION
  • IMMUNOPROPHYLAXIS AND VACCINATION STATUS
  • TREATMENT
  • ANTIMICROBIAL PROPHYLAXIS
  • MANAGEMENT OF OTITIS MEDIA WITH EFFUSION
  • INTRACRANIAL COMPLICATIONS
  • POSSIBLE DEVELOPMENTAL SEQUELAE
  • Chapter 681. Acute Mastoiditis
  • ANATOMY
  • EPIDEMIOLOGY
  • MICROBIOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS AND IMAGING
  • MANAGEMENT
  • SPECIAL SITUATIONS
  • Chapter 682. The Inner Ear and Diseases of the Bony Labyrinth
  • OTHER DISEASES OF THE INNER EAR
  • Chapter 683. Traumatic Injuries of the Ear and Temporal Bone
  • AURICLE AND EXTERNAL AUDITORY CANAL
  • TYMPANIC MEMBRANE AND MIDDLE EAR
  • TEMPORAL BONE FRACTURES
  • ACOUSTIC TRAUMA
  • Chapter 684. Tumors of the Ear and Temporal Bone
  • Part XXIX. The Skin
  • Chapter 685. Morphology of the Skin
  • EPIDERMIS
  • DERMIS
  • SUBCUTANEOUS TISSUE
  • APPENDAGEAL STRUCTURES
  • Chapter 686. Dermatologic Evaluation of the Patient
  • HISTORY AND PHYSICAL EXAMINATION
  • BIOPSY OF SKIN
  • WOOD LAMP
  • POTASSIUM HYDROXIDE PREPARATION
  • TZANCK SMEAR
  • IMMUNOFLUORESCENCE STUDIES
  • 686.1. Cutaneous Manifestations of Systemic Diseases
  • 686.2. Multisystem Medication Reactions
  • Chapter 687. Principles of Dermatologic Therapy
  • WET DRESSINGS
  • BATH OILS, COLLOIDS, AND SOAPS
  • LUBRICANTS
  • SHAMPOOS
  • POWDERS
  • PASTES
  • KERATOLYTIC AGENTS
  • TAR COMPOUNDS
  • ANTIFUNGAL AGENTS
  • TOPICAL ANTIBIOTICS
  • TOPICAL CORTICOSTEROIDS
  • TOPICAL NONSTEROIDAL ANTIINFLAMMATORY AGENTS
  • SUNSCREENS
  • LASER THERAPY
  • Chapter 688. Dermatologic Diseases of the Neonate
  • SEBACEOUS HYPERPLASIA
  • MILIA
  • SUCKING BLISTERS
  • CUTIS MARMORATA
  • HARLEQUIN COLOR CHANGE
  • NEVUS SIMPLEX (SALMON PATCH)
  • CONGENITAL DERMAL MELANOCYTOSIS (SLATE GRAY NEVUS)
  • ERYTHEMA TOXICUM
  • TRANSIENT NEONATAL PUSTULAR MELANOSIS
  • INFANTILE ACROPUSTULOSIS
  • EOSINOPHILIC PUSTULAR FOLLICULITIS
  • Chapter 689. Cutaneous Defects
  • SKIN DIMPLES
  • REDUNDANT SKIN
  • AMNIOTIC CONSTRICTION BANDS
  • PREAURICULAR SINUSES AND PITS
  • ACCESSORY TRAGI
  • BRANCHIAL CLEFT AND THYROGLOSSAL CYSTS AND SINUSES
  • PILONIDAL SINUS AND ABSCESS
  • SUPERNUMERARY NIPPLES
  • APLASIA CUTIS CONGENITA (CONGENITAL ABSENCE OF SKIN)
  • FOCAL FACIAL DERMAL DYSPLASIAS
  • FOCAL DERMAL HYPOPLASIA (GOLTZ-GORLIN SYNDROME)
  • DYSKERATOSIS CONGENITA (ZINSSER-ENGMAN-COLE SYNDROME)
  • CUTIS VERTICIS GYRATA
  • Chapter 690. Ectodermal Dysplasias
  • HYPOHIDROTIC ECTODERMAL DYSPLASIA
  • HIDROTIC ECTODERMAL DYSPLASIA (CLOUSTON SYNDROME)
  • Chapter 691. Vascular Anomalies
  • VASCULAR MALFORMATIONS
  • LYMPHATIC MALFORMATIONS
  • ARTERIOVENOUS MALFORMATION
  • KLIPPEL-TRENAUNAY AND PARKES-WEBER SYNDROMES
  • PHAKOMATOSIS PIGMENTOVASCULARIS
  • NEVUS ANEMICUS
  • VASCULAR TUMORS
  • Chapter 692. Cutaneous Nevi
  • ACQUIRED MELANOCYTIC NEVUS
  • ATYPICAL MELANOCYTIC NEVUS
  • CONGENITAL MELANOCYTIC NEVUS
  • MELANOMA
  • HALO NEVUS
  • SPITZ NEVUS (SPINDLE AND EPITHELIOID CELL NEVUS)
  • ZOSTERIFORM LENTIGINOUS NEVUS (AGMINATED LENTIGINES)
  • NEVUS SPILUS (SPECKLED LENTIGINOUS NEVUS)
  • NEVUS OF OTA AND NEVUS OF ITO
  • BLUE NEVI
  • NEVUS DEPIGMENTOSUS (ACHROMIC NEVUS)
  • EPIDERMAL NEVI
  • NEVUS COMEDONICUS
  • CONNECTIVE TISSUE NEVUS
  • SMOOTH MUSCLE HAMARTOMA
  • Chapter 693. Hyperpigmented Lesions
  • DISORDERS OF PIGMENTATION
  • EPHELIDES (FRECKLES)
  • LENTIGINES
  • CAFÉ-AU-LAIT MACULES
  • INCONTINENTIA PIGMENTI (BLOCH-SULZBERGER DISEASE)
  • POSTINFLAMMATORY PIGMENTARY CHANGES
  • Chapter 694. Hypopigmented Lesions
  • ALBINISM
  • MELANOBLAST MIGRATION ABNORMALITIES
  • Chapter 695. Vesiculobullous Disorders
  • 695.1. Erythema Multiforme
  • 695.2. Reactive Infectious Mucocutaneous Eruption
  • 695.3. Stevens-Johnson Syndrome
  • 695.4. Toxic Epidermal Necrolysis
  • 695.5. Mechanobullous Disorders
  • 695.6. Pemphigus
  • 695.7. Dermatitis Herpetiformis
  • 695.8. Linear Immunoglobulin A (IgA) Dermatosis (Chronic Bullous Dermatosis of Childhood)
  • Chapter 696. Eczematous Disorders
  • 696.1. Contact Dermatitis
  • 696.2. Nummular Eczema
  • 696.3. Pityriasis Alba
  • 696.4. Lichen Simplex Chronicus
  • 696.5. Acute Palmoplantar Eczema
  • 696.6. Seborrheic Dermatitis
  • Chapter 697. Photosensitivity
  • ACUTE SUNBURN REACTION
  • PHOTOSENSITIVE REACTIONS
  • PORPHYRIAS
  • COLLOID MILIUM
  • HYDROA VACCINIFORME
  • SOLAR URTICARIA
  • POLYMORPHOUS LIGHT ERUPTION
  • ACTINIC PRURIGO
  • COCKAYNE SYNDROME
  • XERODERMA PIGMENTOSUM
  • ROTHMUND-THOMSON SYNDROME
  • BLOOM SYNDROME
  • HARTNUP DISEASE
  • Chapter 698. Diseases of the Epidermis
  • 698.1. Psoriasis
  • 698.2. Pityriasis Lichenoides
  • 698.3. Keratosis Pilaris
  • 698.4. Lichen Spinulosus
  • 698.5. Pityriasis Rosea
  • 698.6. Pityriasis Rubra Pilaris
  • 698.7. Darier Disease (Keratosis Follicularis)
  • 698.8. Lichen Nitidus
  • 698.9. Lichen Striatus
  • 698.10. Lichen Planus
  • 698.11. Porokeratosis
  • 698.12. Gianotti-Crosti Syndrome (Papular Acrodermatitis)
  • 698.13. Acanthosis Nigricans
  • Chapter 699. Disorders of Keratinization
  • DISORDERS OF CORNIFICATION
  • COLLODION BABY
  • NONSYNDROMIC ICHTHYOSES
  • AUTOSOMAL RECESSIVE CONGENITAL ICHTHYOSES
  • KERATINOPATHIC ICHTHYOSES
  • OTHER NONSYNDROMIC ICHTHYOSES
  • SYNDROMIC ICHTHYOSES
  • OTHER SYNDROMES WITH ICHTHYOSIS
  • Chapter 700. Diseases of the Dermis
  • KELOID
  • 700.1. Mast Cell Activation Syndrome
  • Chapter 701. Diseases of Subcutaneous Tissue
  • CORTICOSTEROID-INDUCED ATROPHY
  • Raynaud Phenomenon
  • 701.1. Panniculitis and Erythema Nodosum
  • 701.2. Lipodystrophy
  • Chapter 702. Disorders of the Sweat Glands
  • ANHIDROSIS
  • HYPERHIDROSIS
  • MILIARIA
  • BROMHIDROSIS
  • HIDRADENITIS SUPPURATIVA
  • FOX-FORDYCE DISEASE
  • Chapter 703. Disorders of Hair
  • HYPERTRICHOSIS
  • HYPOTRICHOSIS AND ALOPECIA
  • TRAUMATIC ALOPECIA (TRACTION ALOPECIA, HAIR PULLING, TRICHOTILLOMANIA)
  • ALOPECIA AREATA
  • ACQUIRED DIFFUSE HAIR LOSS
  • CONGENITAL DIFFUSE HAIR LOSS
  • Chapter 704. Disorders of the Nails
  • ABNORMALITIES IN NAIL SHAPE OR SIZE
  • CHANGES IN NAIL COLOR
  • NAIL SEPARATION
  • NAIL CHANGES ASSOCIATED WITH SKIN DISEASE
  • TRACHYONYCHIA (20-NAIL DYSTROPHY)
  • NAIL INFECTION
  • PARONYCHIAL INFLAMMATION
  • PARONYCHIAL TUMORS
  • Chapter 705. Disorders of the Mucous Membranes
  • ANGULAR CHEILITIS
  • APHTHOUS STOMATITIS (CANKER SORES)
  • FORDYCE SPOTS
  • EPSTEIN PEARLS (GINGIVAL CYSTS OF THE NEWBORN)
  • MUCOCELE
  • FISSURED TONGUE
  • GEOGRAPHIC TONGUE (BENIGN MIGRATORY GLOSSITIS)
  • BLACK HAIRY TONGUE
  • ORAL HAIRY LEUKOPLAKIA
  • ACUTE NECROTIZING ULCERATIVE GINGIVITIS (VINCENT STOMATITIS, FUSOSPIROCHETAL GINGIVITIS, TRENCH MOUTH)
  • NOMA
  • PTEN HAMARTOMA SYNDROME (COWDEN SYNDROME)
  • Chapter 706. Cutaneous Bacterial Infections
  • 706.1. Impetigo
  • 706.2. Subcutaneous Tissue Infections
  • 706.3. Staphylococcal Scalded Skin Syndrome (Ritter Disease)
  • 706.4. Ecthyma
  • 706.5. Other Cutaneous Bacterial Infections
  • Chapter 707. Cutaneous Fungal Infections
  • TINEA VERSICOLOR
  • DERMATOPHYTOSES
  • CANDIDAL INFECTIONS (CANDIDIASIS AND MONILIASIS)
  • Chapter 708. Cutaneous Viral Infections
  • WART (VERRUCA)
  • MOLLUSCUM CONTAGIOSUM
  • Chapter 709. Arthropod Bites and Infestations
  • 709.1. Arthropod Bites
  • 709.2. Scabies
  • 709.3. Pediculosis
  • 709.4. Seabather’s Eruption
  • Chapter 710. Acne
  • ACNE VULGARIS
  • DRUG-INDUCED ACNE
  • NEONATAL CEPHALIC PUSTULOSIS (FORMERLY NEONATAL ACNE)
  • INFANTILE ACNE
  • MID-CHILDHOOD ACNE
  • ACNE FULMINANS (ACUTE FEBRILE ULCERATIVE ACNE)
  • Chapter 711. Tumors of the Skin
  • INFUNDIBULAR FOLLICULAR CYST
  • MILIUM
  • FIBROFOLLICULOMAS
  • PILAR CYST (TRICHILEMMAL CYST)
  • PILOMATRICOMA (PILOMATRIXOMA)
  • TRICHOEPITHELIOMA
  • ERUPTIVE VELLUS HAIR CYSTS
  • STEATOCYSTOMA MULTIPLEX
  • SYRINGOMA
  • INFANTILE DIGITAL FIBROMA
  • DERMATOFIBROMA
  • JUVENILE XANTHOGRANULOMA
  • LIPOMA
  • BASAL CELL CARCINOMA
  • NEVOID BASAL CELL CARCINOMA SYNDROME (BASAL CELL NEVUS SYNDROME, GORLIN SYNDROME)
  • MELANOMA
  • MUCOSAL NEUROMA SYNDROME (MULTIPLE ENDOCRINE NEOPLASIA TYPE IIB)
  • Chapter 712. Nutritional Dermatoses
  • OVERVIEW
  • ACRODERMATITIS ENTEROPATHICA
  • ESSENTIAL FATTY ACID DEFICIENCY
  • KWASHIORKOR
  • CYSTIC FIBROSIS
  • PELLAGRA
  • SCURVY (VITAMIN C OR ASCORBIC ACID DEFICIENCY)
  • VITAMIN A DEFICIENCY
  • Bone and Joint Disorders
  • Section 1. Orthopedic Problems
  • Chapter 713. Orthopedic Growth and Development
  • IN UTERO POSITIONING
  • GROWTH AND DEVELOPMENT
  • CENTERS OF OSSIFICATION
  • GAIT/FUNCTIONAL MATURATION
  • Chapter 714. Orthopedic Evaluation of the Child
  • HISTORY
  • PHYSICAL EXAMINATION
  • NEUROLOGIC EVALUATION
  • LIMPING
  • BACK PAIN
  • RADIOGRAPHIC ASSESSMENT
  • LABORATORY STUDIES
  • Chapter 715. The Foot and Toes
  • 715.1. Metatarsus Adductus
  • 715.2. Calcaneovalgus Feet
  • 715.3. Talipes Equinovarus (Clubfoot)
  • 715.4. Congenital Vertical Talus
  • 715.5. Hypermobile Pes Planus (Flexible Flatfeet)
  • 715.6. Tarsal Coalition
  • 715.7. Cavus Feet
  • 715.8. Osteochondroses/Apophysitis
  • 715.9. Puncture Wounds of the Foot
  • 715.10. Toe Deformities
  • 715.11. Painful Foot
  • 715.12. Shoes
  • Chapter 716. Torsional and Angular Deformities of the Limb
  • 716.1. Normal Limb Development
  • 716.2. Limb Evaluation
  • 716.3. Torsional Deformities
  • 716.4. Coronal Plane Deformities
  • 716.5. Congenital Angular Deformities of the Tibia and Fibula
  • Chapter 717. Leg-Length Discrepancy
  • DIAGNOSIS AND CLINICAL FINDINGS
  • RADIOGRAPHIC EVALUATION
  • TREATMENT
  • Chapter 718. The Knee
  • NORMAL DEVELOPMENT OF THE KNEE
  • ANATOMY AND RANGE OF MOTION
  • 718.1. Discoid Lateral Meniscus
  • 718.2. Popliteal Cysts (Baker Cysts)
  • 718.3. Juvenile Osteochondritis Dissecans
  • 718.4. Osgood-Schlatter Disease and Sinding-Larsen-Johansson Syndrome
  • 718.5. Patellofemoral Pain Syndrome
  • 718.6. Patellofemoral Instability
  • 718.7. Anterior Cruciate Ligament Rupture
  • Chapter 719. The Hip
  • GROWTH AND DEVELOPMENT
  • VASCULAR SUPPLY
  • 719.1. Developmental Dysplasia of the Hip
  • 719.2. Transient Monoarticular Synovitis (Toxic Synovitis)
  • 719.3. Legg-Calvé-Perthes Disease
  • 719.4. Slipped Capital Femoral Epiphysis
  • Chapter 720. The Spine
  • NORMAL SPINAL CURVATURES
  • OVERVIEW OF ABNORMAL SPINAL CURVATURES
  • 720.1. Idiopathic Scoliosis
  • 720.2. Congenital Scoliosis
  • 720.3. Neuromuscular Scoliosis, Genetic Syndromes, and Compensatory Scoliosis
  • 720.4. Kyphosis
  • 720.5. Back Pain in Children
  • 720.6. Spondylolysis and Spondylolisthesis
  • 720.7. Spine Infection
  • 720.8. Intervertebral Disk Herniation/Slipped Vertebral Apophysis
  • 720.9. Tumors
  • Chapter 721. The Neck
  • 721.1. Torticollis
  • 721.2. Klippel-Feil Syndrome
  • 721.3. Cervical Anomalies and Instabilities
  • Chapter 722. The Upper Limb
  • SHOULDER
  • ELBOW
  • WRIST
  • HAND
  • Chapter 723. Arthrogryposis
  • ETIOLOGY
  • CLASSIFICATION
  • MANAGEMENT OF ORTHOPEDIC PROBLEMS OF ARTHROGRYPOSIS
  • FOOT PROBLEMS
  • KNEE PROBLEMS
  • HIP PROBLEMS
  • UPPER EXTREMITY PROBLEMS
  • Chapter 724. Common Fractures
  • 724.1. Unique Characteristics of Pediatric Fractures
  • 724.2. Pediatric Fracture Patterns
  • 724.3. Upper Extremity Fractures
  • 724.4. Lower Extremity Fractures
  • 724.5. Operative Treatment of Fractures
  • 724.6. Complications of Fractures in Children
  • Chapter 725. Osteomyelitis
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • RADIOGRAPHIC EVALUATION
  • DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • Chapter 726. Septic Arthritis
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • DIFFERENTIAL DIAGNOSIS
  • TREATMENT
  • PROGNOSIS
  • Section 2. Sports Medicine
  • Chapter 727. Prevention of Injuries
  • PREPARTICIPATION SPORTS EXAMINATION
  • Chapter 728. Management of Musculoskeletal Injury
  • MECHANISM OF INJURY
  • 728.1. Growth Plate Injuries
  • 728.2. Shoulder Injuries
  • 728.3. Elbow Injuries
  • 728.4. Low Back Injuries
  • 728.5. Hip and Pelvis Injuries
  • 728.6. Knee Injuries
  • 728.7. Lower Leg Exertional Pain: Shin Splints, Stress Fractures, and Chronic Compartment Syndrome
  • 728.8. Ankle Injuries
  • 728.9. Foot Injuries
  • Chapter 729. Sports-Related Traumatic Brain Injury (Concussion)
  • DEFINITION/TERMINOLOGY
  • EPIDEMIOLOGOY
  • PATHOPHYSIOLOGY
  • SIGNS AND SYMPTOMS
  • INITIAL ASSESSMENT AND TOOLS
  • MANAGEMENT
  • COMPLICATIONS/LONG-TERM EFFECTS
  • PREVENTION
  • Chapter 730. Cervical Spine Injuries
  • SOFT TISSUE INJURY
  • SPEAR TACKLER’S SPINE
  • CERVICAL FRACTURES
  • STINGERS (BURNERS)
  • BURNING HANDS SYNDROME
  • TRANSIENT QUADRIPARESIS
  • CONGENITAL SPINAL STENOSIS
  • SPINAL CORD INJURY
  • Chapter 731. Heat Injuries
  • Chapter 732. Nutrition and Endocrine Conditions in Athletes
  • Chapter 733. Performance-Enhancing Aids
  • Chapter 734. Specific Sports and Associated Injuries
  • SPORTS PARTICIPATION, EARLY SPECIALIZATION, INJURY RISK, AND BURNOUT
  • FOOTBALL
  • BASEBALL/SOFTBALL
  • BASKETBALL/VOLLEYBALL
  • TENNIS
  • LACROSSE
  • SWIMMING/DIVING
  • SOCCER
  • ICE HOCKEY
  • FIELD HOCKEY
  • SKIING AND SNOWBOARDING
  • SKATEBOARDING
  • CYCLING AND MOTOCROSS
  • WRESTLING
  • RUNNING
  • CHEERLEADING
  • GYMNASTICS
  • DANCE
  • ADAPTIVE SPORTS
  • Section 3. The Skeletal Dysplasias
  • Chapter 735. General Considerations in Skeletal Dysplasias
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • MOLECULAR GENETICS OF SKELETAL DYSPLASIAS
  • PATHOPHYSIOLOGY
  • TREATMENT
  • Chapter 736. Disorders Involving Cartilage Matrix Proteins
  • TYPE 2 COLLAGENOPATHIES
  • KNIEST DYSPLASIA
  • PSEUDOACHONDROPLASIA AND MULTIPLE EPIPHYSEAL DYSPLASIA
  • SCHMID METAPHYSEAL DYSPLASIA
  • Chapter 737. Disorders Involving Transmembrane Receptors
  • FGFR3 CHONDRODYSPLASIA GROUP
  • JANSEN METAPHYSEAL DYSPLASIA
  • Chapter 738. Disorders Involving Ion Transporters
  • AUTOSOMAL RECESSIVE MULTIPLE EPIPHYSEAL DYSPLASIA
  • Chapter 739. Disorders Involving Transcription Factors
  • CAMPOMELIC DYSPLASIA
  • CLEIDOCRANIAL DYSPLASIA
  • SHOX GENE-RELATED CONDITIONS
  • NAIL-PATELLA SYNDROME
  • Chapter 740. Osteopetrosis and Other Disorders Involving Defective Bone Resorption
  • OSTEOPETROSIS
  • CLINICAL MANIFESTATIONS
  • TREATMENT
  • PYCNODYSOSTOSIS AND DYSOSTEOSCLEROSIS
  • Chapter 741. Other Inherited Disorders of Skeletal Development
  • ELLIS-VAN CREVELD SYNDROME
  • ASPHYXIATING THORACIC DYSTROPHY
  • SHORT-RIB POLYDACTYLY SYNDROMES
  • CARTILAGE-HAIR HYPOPLASIA-ANAUXETIC SPECTRUM DISORDERS
  • TRPV4-SPECTRUM DISORDERS
  • METATROPIC DYSPLASIA
  • SPONDYLOMETAPHYSEAL DYSPLASIA, KOZLOWSKI TYPE
  • DISORDERS INVOLVING FILAMINS
  • JUVENILE OSTEOCHONDROSES
  • CAFFEY DISEASE (INFANTILE CORTICAL HYPEROSTOSIS)
  • FIBRODYSPLASIA OSSIFICANS PROGRESSIVA
  • Chapter 742. Osteogenesis Imperfecta
  • ETIOLOGY
  • EPIDEMIOLOGY
  • PATHOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • LABORATORY FINDINGS
  • COMPLICATIONS
  • TREATMENT
  • PROGNOSIS
  • GENETIC COUNSELING
  • Section 4. Connective Tissue Disorders
  • Chapter 743. Marfan Syndrome
  • EPIDEMIOLOGY
  • PATHOGENESIS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • DIFFERENTIAL DIAGNOSIS
  • LABORATORY FINDINGS
  • MANAGEMENT
  • CURRENT THERAPIES
  • PROGNOSIS
  • GENETIC COUNSELING
  • Chapter 744. Ehlers-Danlos Syndrome
  • CLASSIFICATION OF THE SIX MOST COMMON SUBTYPES OF EHLERS-DANLOS SYNDROME
  • DIFFERENTIAL DIAGNOSIS
  • GENERAL APPROACH TO MANAGEMENT
  • Chapter 745. Cutis Laxa
  • CLINICAL MANIFESTATIONS
  • HISTOLOGY
  • TREATMENT
  • Section 5. Metabolic Bone Disease
  • Chapter 746. Bone Structure, Growth, and Hormonal Regulation
  • Chapter 747. Hypophosphatasia
  • Chapter 748. Hyperphosphatasia
  • Chapter 749. Osteoporosis
  • Part XXXI. Rehabilitation Medicine
  • Chapter 750. Rehabilitation for Traumatic Brain Injury
  • PATHOPHYSIOLOGY
  • SEVERITY
  • MEDICAL COMPLICATIONS
  • OUTCOME ASSOCIATED WITH SEVERE TRAUMATIC BRAIN INJURY
  • Chapter 751. Spinal Cord Injury and Autonomic Dysreflexia Management
  • CLINICAL MANIFESTATIONS
  • PROGNOSIS
  • Chapter 752. Spasticity
  • SYSTEMIC MEDICATIONS
  • INJECTION MANAGEMENT
  • SURGICAL MANAGEMENT
  • Chapter 753. Birth Brachial Plexus Palsy
  • PHYSICAL EXAMINATION
  • EVALUATION
  • TREATMENT
  • Chapter 754. Meningomyelocele (Spina Bifida)
  • ETIOLOGY
  • PREVENTION
  • PRENATAL SCREENING
  • CLINICAL IMPLICATIONS
  • ADOLESCENCE AND TRANSITION TO ADULTHOOD
  • Chapter 755. Upper and Lower Extremity Assistive Devices
  • ORTHOSES
  • PROSTHESES
  • ASSISTIVE MOBILITY DEVICES
  • WHEELCHAIR
  • ROBOTIC DEVICES
  • Chapter 756. Health and Wellness for Children with Disabilities
  • DISABILITY
  • Part XXXII. Environmental Health
  • Chapter 757. Overview of Environmental Health and Children
  • GLOBAL CLIMATE CHANGE
  • LOCALIZED ENVIRONMENTAL HAZARDS
  • TOXINS VERSUS TOXICANTS
  • MYCOTOXINS
  • FOOD-BORNE DISEASES CAUSED BY ENVIRONMENTAL EXPOSURES
  • Chapter 758. Biologic Effects of Ionizing Radiation on Children
  • DIAGNOSTIC IMAGING, RADIATION THERAPY
  • BIOLOGIC EFFECTS OF RADIATION
  • RADIATION EXPOSURE IN DIAGNOSTIC IMAGING OF CHILDREN
  • DECREASING UNNECESSARY DIAGNOSTIC RADIATION IN CHILDREN WHILE STILL OBTAINING DIAGNOSTIC IMAGES
  • RADIATION THERAPY: ACUTE AND LATE EFFECTS
  • WHOLE BODY IRRADIATION
  • INTERNAL CONTAMINATION
  • EXTERNAL CONTAMINATION
  • Chapter 759. Chemical Pollutants
  • SYNTHETIC CHEMICALS AND HUMAN HEALTH
  • 759.1. Tobacco
  • 759.2. Marijuana Smoke Exposure
  • Chapter 760. Heavy Metal Intoxication
  • ARSENIC
  • MERCURY
  • TREATMENT OF ARSENIC AND MERCURY INTOXICATION
  • Chapter 761. Lead Poisoning
  • PUBLIC HEALTH HISTORY
  • SOURCES OF EXPOSURE
  • METABOLISM
  • CLINICAL EFFECTS
  • CLINICAL SYMPTOMS
  • DIAGNOSIS
  • TREATMENT
  • Chapter 762. Nonbacterial Food Poisoning
  • 762.1. Mushroom Poisoning
  • 762.2. Solanine Poisoning
  • 762.3. Seafood Poisoning
  • 762.4. Melamine Poisoning
  • Chapter 763. Biological and Chemical Terrorism
  • ETIOLOGY
  • EPIDEMIOLOGY AND PEDIATRIC-SPECIFIC CONCERNS
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • PREVENTION
  • TREATMENT
  • Chapter 764. Mass Psychogenic Illness
  • CLINICAL FEATURES AND DIAGNOSIS
  • TREATMENT STRATEGIES
  • Chapter 765. Animal and Human Bites
  • EPIDEMIOLOGY
  • CLINICAL MANIFESTATIONS
  • DIAGNOSIS
  • COMPLICATIONS
  • TREATMENT
  • PREVENTION
  • Chapter 766. Rat Bite Fever
  • ETIOLOGY
  • CLINICAL COURSE
  • DIAGNOSIS
  • TREATMENT
  • Chapter 767. Mpox (Monkeypox)
  • CLINICAL COURSE
  • PREVENTION AND TREATMENT
  • Chapter 768. Envenomations
  • GENERAL APPROACH TO THE ENVENOMATED CHILD
  • SNAKE BITES
  • SPIDER BITES
  • SCORPION STINGS
  • HYMENOPTERA STINGS
  • MARINE ENVENOMATION
  • Part XXXIII. Laboratory Medicine (available in digital format only)
  • Chapter 769. Laboratory Testing in Infants and Children
  • COMMON CHALLENGES IN PEDIATRIC LABORATORY MEDICINE
  • ACCURACY AND PRECISION OF LABORATORY TESTS
  • SENSITIVITY, ACCURACY, AND ANALYTIC TESTING
  • PREDICTIVE VALUE OF LABORATORY TESTS
  • NEONATAL SCREENING TESTS
  • TESTING IN REFINING A DIFFERENTIAL DIAGNOSIS
  • Chapter 770. Reference Intervals for Laboratory Tests and Procedures
  • Index
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