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  • Biliary atresia - Symptoms, diagnosis and treatment - BMJ Best Practice
    Biliary atresia should be suspected in any baby with jaundice and pale stools, jaundice persisting beyond 14 days of age, or if the direct or conjugated bilirubin is > 17 1 micromoles L (1 mg dL) Hepatoportoenterostomy is warranted in infants aged <100 days and without evidence of end-stage liver disease, but many go on to require liver transplantation within a few years
  • Biliary atresia - Symptoms, diagnosis and treatment - BMJ Best Practice
    Biliary atresia should be suspected in any baby with jaundice and pale stools, jaundice persisting beyond 14 days of age, or if the direct or conjugated bilirubin is >1 mg dL Hepatoportoenterostomy is warranted in infants aged <100 days of age and without evidence of end-stage liver disease, but many go on to require liver transplantation within a few years
  • Atresia das vias biliares - Sintomas, diagnóstico e tratamento | BMJ . . .
    A atresia das vias biliares é uma doença grave que requer um diagnóstico precoce e imediato, preferivelmente antes de 6-8 semanas de idade Uma obstrução fibro-obliterativa da árvore biliar extra-hepática que evolui para os ductos intra-hepáticos; pode se desenvolver no útero ou durante o período neonatal
  • Symptoms, diagnosis and treatment - BMJ Best Practice
    Acute cholangitis is an infection of the biliary tree that requires prompt diagnosis and treatment Most patients with acute cholangitis have fever, jaundice, and right upper quadrant pain (Charcot's triad) Acute cholangitis can quickly become an acute, septic, life-threatening infection that requires rapid evaluation and treatment
  • Primary biliary cholangitis - Symptoms, diagnosis and treatment | BMJ . . .
    Primary biliary cholangitis (PBC) is characterised by progressive intrahepatic bile duct damage and loss PBC is significantly more common in women than in men Peak incidence is around age 40 years, and median age at diagnosis is 65 years The combination of a cholestatic pattern of serum liver
  • Esophageal atresia and tracheoesophageal fistula - BMJ Best Practice
    Esophageal atresia (EA) and tracheoesophageal fistula (TEF) are congenital malformations that result from the defective separation of the common embryonic precursor to both the esophagus and trachea The most common type is a blind-ending upper esophageal pouch with a fistulous connection between the distal esophageal segment and the trachea
  • Gastroenterology and hepatology - BMJ Best Practice
    Primary biliary cholangitis; Primary sclerosing cholangitis; Pyloric stenosis; R Rotor syndrome; S Salmonellosis; Shigella infection; Short bowel syndrome; Small bowel obstruction; Spontaneous bacterial peritonitis; Steatotic liver disease; Stomach cancer; Strongyloides infection; T Tapeworm infection; Toxic colitis and toxic megacolon
  • Wilms tumour - Symptoms, diagnosis and treatment - BMJ Best Practice
    Wilms' tumour, or nephroblastoma, is the most common form of renal malignancy in childhood Nakata K, Colombet M, Stiller CA, et al Incidence of childhood renal tumours: an international population-based study


















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