Biliary atresia presents as an obliterative cholangiopathy with neonatal jaundice and pale
stools. The disease exhibits aetiological heterogeneity with a multiplicity of potential …

Neonatal cholestasis is a group of rare disorders of impaired bile flow characterized by
conjugated hyperbilirubinaemia in the newborn and young infant. Neonatal cholestasis is …

Cholestatic jaundice in infancy affects approximately 1 in every 2500 term infants and is
infrequently recognized by primary providers in the setting of physiologic jaundice …

This guideline refers to infants, children, and adolescents ages 0 to 18 years. The areas
covered include indications for diagnostic and therapeutic esophagogastroduodenoscopy …

Biliary Atresia and other cholestatic childhood diseases are rare conditions affecting the
function and/or anatomy along the canalicular-bile duct continuum, characterised by onset of …

Biliary atresia (BA) remains an enigmatic disease with a degree of etiologic heterogeneity. A
number of variants can be defined clinically, and these include the syndromic group …

Neonatal cholestasis is characterized by conjugated hyperbilirubinemia in the newborn and
young infant and is a sign common to over 100 hepatobiliary and/or metabolic disorders. A …

Cholestatic jaundice in early infancy is a complex diagnostic problem. Misdiagnosis of
cholestasis as physiologic jaundice delays the identification of severe liver diseases. In the …

Biliary atresia (BA) is a rare and severe inflammatory and obliterative cholangiopathy that
affects both extra-and intrahepatic bile ducts. BA symptoms occur shortly after birth with …

Advances in endoscopy and anesthesia have enabled gastrointestinal endoscopy for
children since 1960. Over the past decades, the number of endoscopies has increased …