Congenital biliary atresia has several types, including intrahepatic, extrahepatic, and common bile duct types. Infants often show jaundice symptoms within 2 to 3 weeks after birth, with normal stool color, which may be misdiagnosed as physiological jaundice.
Congenital biliary atresia is a congenital developmental disorder characterized by severe jaundice, which may lead to biliary hepatitis and liver cirrhosis.
The cause of neonatal biliary atresia is the gradual fibrosis of the common bile duct, leading to obstruction of the biliary system.
Brief Description
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What is Neonatal Biliary Atresia?
