🍞 A 2-year-old with chronic diarrhoea, abdominal distension, iron deficiency. Antibody test?
IgA tissue transglutaminase (tTG); if positive → duodenal biopsy (Marsh grade). Coeliac disease.
🟡 A 6-week-old with pale stools, conjugated bilirubinaemia. Next step?
Urgent abdominal ultrasound and referral to paediatric hepatology for possible biliary atresia.
🧂 A child with cystic fibrosis and steatorrhoea. Enzyme replacement?
Pancreatic enzyme replacement therapy (PERT; Creon) dosed per fat intake, with PPI to improve efficacy.
🩸 A 12-year-old with bloody diarrhoea, tenesmus, weight loss. Most likely diagnosis?
Ulcerative colitis – endoscopic continuous inflammation from rectum, confirm with colonoscopy + biopsies.
💊 First-line treatment for Crohn disease with moderate-severe ileocolitis?
Exclusive enteral nutrition (EEN) for 6–8 weeks; corticosteroids (prednisolone/budesonide) or anti-TNF (infliximab) in refractory.
⚠️ A neonate with bilious vomiting and abdominal distension. Most important next step?
Upper GI contrast study to exclude malrotation with volvulus – surgical emergency.
🧪 Most accurate non-invasive test to rule out coeliac disease in IgA-sufficient child?
IgA tTG (sensitivity >95%); if weak positive, confirm with EMA and HLA-DQ2/DQ8.
🩺 Treatment of hepatic encephalopathy in a child with cirrhosis?
Lactulose (oral/enema) to reduce ammonia; protein restriction avoided; manage precipitating factors (infection, bleeding, constipation).
🏥 A 14-year-old with dysphagia, food impaction, atopy. Suspected disorder?
Eosinophilic oesophagitis (EoE). Diagnosis by oesophageal biopsy (≥15 eosinophils/HPF). Treatment: PPI, swallowed topical steroids (budesonide/fluticasone).
🧫 A child with jaundice, hepatosplenomegaly, Kayser–Fleischer rings. Diagnostic test?
Serum ceruloplasmin, urinary copper, slit-lamp examination; Wilson disease – treat with zinc/chelators.