The metabolite of bile draining into the intestine is bilirubin, which gives the faeces a yellow-green colour. In children with biliary atresia, the bile does not drain smoothly into the…
Without surgical treatment, the child will develop cirrhosis within 6 months and progress to liver failure within 1 year and die within 2 years of age.
There are more available experimental methods, but all have poor specificity. In biliary atresia, total serum bilirubin is increased, and the proportion of one-minute bilirubin is correspondingly increased. The abnormally…
Biliary atresia is a common disease that poses a serious health risk to newborns, and 95% of patients are “untreatable”. Since the introduction of the Kasai procedure, which originated in…
Biliary atresia is the most common cause of neonatal cholestasis and is characterized by complete fibrotic obstruction of part or all of the extrahepatic biliary tract occurring within the first…
Biliary atresia is a condition in which part or all of the extrahepatic bile duct is occluded at the end of pregnancy, at birth, or after birth, and bile cannot…
Biliary atresia (BA) and infant hepatitis syndrome (IHS) are common causes of obstructive jaundice in newborns and infants. Infant hepatitis syndrome is an infection of the liver or a metabolic…
Biliary atresia as a type of hepatobiliary disease poses a serious threat to the lives of newborn infants. With the continuous development of hepatic hilar-jejunostomy (Kasai procedure), the treatment of…
laparoscopic exploration showed marked cirrhosis of the liver with nodular surface The diagnosis of biliary atresia was confirmed by poorly developed gallbladder seen laparoscopically and no normal bile seen by puncture The…
The survival period for congenital biliary atresia is determined by the child’s physical condition, the presence of complications, and the treatment. If the child has developed gastrointestinal hemorrhage, hepatic encephalopathy and…