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HIGH YIELD NOTES ~5 min read

Core Concepts

Pediatrics covers growth, development, and health from birth through adolescence. Key areas include well-child visits, vaccinations, developmental milestones, common childhood illnesses, and emergent conditions. Growth is monitored via standardized growth charts (weight, height/length, head circumference), while development is assessed using age-appropriate milestones. Prevention is central, with universal newborn screening and adherence to the CDC's immunization schedule being paramount. Common etiologies of illness often differ from adults (e.g., viral causes predominant in respiratory infections, genetic syndromes, congenital anomalies). Family-centered care and consideration of psychosocial factors are crucial.

Clinical Presentation

  • Neonatal Jaundice: Yellow skin/sclera, direct hyperbilirubinemia is always pathologic.
  • Bronchiolitis (RSV): <2 years, viral prodrome, wheezing, tachypnea, retractions.
  • Croup (Laryngotracheobronchitis): Barking cough, inspiratory stridor, hoarseness, often viral.
  • Asthma: Recurrent wheezing, cough (worse at night/with activity), shortness of breath, chest tightness.
  • Febrile Seizures: 6 months - 5 years, generalized tonic-clonic seizure with fever, no CNS infection.
  • Pyloric Stenosis: 2-8 weeks old, non-bilious projectile vomiting after feeds, often hungry post-emesis.
  • Intussusception: 3 months - 3 years, sudden onset intermittent colicky abdominal pain, "currant jelly" stools, sausage-shaped abdominal mass.
  • Hirschsprung Disease: Failure to pass meconium in first 24-48 hours, chronic constipation, abdominal distension.
  • Appendicitis: Periumbilical pain migrating to RLQ, anorexia, nausea, vomiting, fever.
  • UTI: Infants: fever without source, poor feeding, irritability. Older children: dysuria, frequency, urgency, enuresis.
  • Kawasaki Disease: Fever >5 days + 4/5 criteria: conjunctivitis, rash, adenopathy, strawberry tongue/oral changes, hand/foot changes.
  • Henoch-Schönlein Purpura (HSP): Palpable purpura (buttocks/legs), arthritis, abdominal pain, renal involvement (hematuria/proteinuria).
  • Minimal Change Disease (Nephrotic Syndrome): Periorbital edema, ascites, generalized edema, frothy urine.
  • Post-streptococcal Glomerulonephritis (PSGN): 1-3 weeks post strep infection, gross hematuria, edema, hypertension.
  • Meningitis: Fever, lethargy, irritability, poor feeding, bulging fontanelle (infants); headache, stiff neck, photophobia (older children).

Diagnosis (Gold Standard)

Growth/developmental assessment uses CDC growth charts and standardized screening tools (e.g., ASQ-3). Newborn screening varies by state but typically includes metabolic disorders (e.g., PKU, congenital hypothyroidism, galactosemia), hemoglobinopathies (e.g., sickle cell disease), and cystic fibrosis. Specific gold standards include:
Pyloric Stenosis: Abdominal Ultrasound (target sign, elongated/thickened pylorus).
Intussusception: Abdominal Ultrasound (target/pseudokidney sign), Air Enema (diagnostic and therapeutic).
Hirschsprung Disease: Rectal Biopsy (absence of ganglion cells in submucosal and myenteric plexuses).
UTI: Urine Culture (from catheterized sample in infants/young children, midstream clean catch in older children).
Meningitis: Lumbar Puncture with CSF analysis.
Cystic Fibrosis: Sweat Chloride Test.
Lead Poisoning: Serum Lead Level.

Management (First Line)

Vaccinations: Adhere to ACIP/CDC schedule.
Bronchiolitis: Supportive care (hydration, nasal suctioning). Bronchodilators, steroids, and antibiotics are NOT recommended.
Croup: Dexamethasone (single oral dose) for mild-moderate; Racemic Epinephrine for moderate-severe stridor at rest.
Asthma: Albuterol (SABA) for acute exacerbations; Inhaled Corticosteroids (ICS) for long-term control.
Febrile Seizures: Reassurance, antipyretics (no proven benefit in preventing recurrence).
Pyloric Stenosis: Fluid/electrolyte resuscitation, then surgical pyloromyotomy.
Intussusception: Air enema (reduces 75-90%); surgical reduction if enema fails or peritonitis present.
Hirschsprung Disease: Surgical resection of aganglionic segment.
Appendicitis: Surgical appendectomy.
UTI: Empiric oral or IV antibiotics (e.g., Ceftriaxone, Cefixime, Bactrim) based on age/severity, for 7-14 days.
Kawasaki Disease: IVIG + High-dose Aspirin.
HSP: Supportive care. Steroids for severe abdominal pain or joint symptoms. Renal follow-up.
Minimal Change Disease: Oral corticosteroids (e.g., Prednisone).
PSGN: Supportive care (fluid restriction, diuretics for edema, antihypertensives for HTN).
Meningitis: IV antibiotics (Ceftriaxone + Vancomycin, add Ampicillin for neonates); Dexamethasone for H. flu type B.
Anaphylaxis: IM Epinephrine.

Exam Red Flags

  • Fever without a source in infants <3 months: Always work up for sepsis (LP, UA, blood culture).
  • Abnormal Red Reflex: Suspect retinoblastoma or congenital cataracts.
  • Lack of Social Smile by 2 months, Rolling over by 6 months, Walking by 18 months, First words by 15 months: Developmental delay.
  • Non-bilious projectile vomiting in a young infant: Pyloric stenosis.
  • Currant jelly stools + intermittent colicky pain: Intussusception.
  • Barking cough + inspiratory stridor: Croup (acute onset, worse at night).
  • Drooling + Tripoding + Acute stridor/dysphagia: Epiglottitis (rare but life-threatening).
  • Inconsistent history for injury, multiple fractures in different stages of healing, metaphyseal fractures, retinal hemorrhages: Child abuse.
  • Severe unilateral scrotal pain + absent cremasteric reflex: Testicular torsion (surgical emergency).
  • Sudden onset limp + hip pain: Rule out septic arthritis (medical emergency), SCFE, Legg-Calve-Perthes, transient synovitis.
  • Fatigue, Pallor, Pica, Developmental Delay: Iron deficiency anemia.

Sample Practice Questions

Question 1

A 10-year-old boy is brought to the clinic by his parents due to concerns about his short stature. He is consistently in the 5th percentile for height, but his growth velocity has been normal for his age over the past year. He denies headaches, vision changes, or chronic illnesses. Both parents recall being 'late bloomers' and having pubertal development later than their peers. His physical exam is otherwise unremarkable, and there are no signs of puberty. Bone age radiography shows a bone age of 8 years. What is the most likely diagnosis?

A) Growth hormone deficiency
B) Hypothyroidism
C) Familial short stature
D) Constitutional growth delay
Explanation: This area is hidden for preview users.
Question 2

A 10-year-old boy presents with a 2-week history of fatigue, dark-colored urine, and swelling around his eyes and ankles. He recently recovered from a 'strep throat' infection, which was treated with a 5-day course of amoxicillin. On examination, his blood pressure is 145/95 mmHg, and he has periorbital and pedal edema. Urinalysis shows proteinuria (3+), hematuria (red blood cell casts present), and specific gravity 1.025. Serum creatinine is 1.5 mg/dL (elevated for age), and C3 complement levels are low. What is the most likely diagnosis?

A) Nephrotic syndrome
B) IgA nephropathy
C) Acute post-streptococcal glomerulonephritis (APSGN)
D) Hemolytic-uremic syndrome (HUS)
Explanation: This area is hidden for preview users.
Question 3

A 4-week-old full-term male infant is brought to the emergency department by his mother due to progressively worsening non-bilious projectile vomiting for the past week. The vomiting typically occurs shortly after feeding, and the infant appears hungry immediately afterward. He has had fewer wet diapers and seems more irritable. On examination, the infant is lethargic, has dry mucous membranes, and has decreased skin turgor. His weight is below his birth weight. A firm, olive-shaped mass is palpable in the epigastrium. Laboratory results show hypochloremic, hypokalemic metabolic alkalosis. Which of the following is the most appropriate next diagnostic step?

A) Upper gastrointestinal series with barium contrast
B) Abdominal ultrasound
C) Stool guaiac test
D) Sweat chloride test
Explanation: This area is hidden for preview users.

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