Congenital biliary atresia is a rare disease of the liver and biliary tract, characterized by disruption or deficiency of the extrahepatic biliary system, causing obstruction of bile flow. Due to misdiagnosis and late detection, many infants are missed the golden opportunity to have surgery to treat the disease. So when is the best time to treat congenital biliary atresia?

Physiological jaundice is a common sign in newborns, caused by broken red blood cells and incomplete liver function of bilirubin metabolism. However, jaundice due to biliary atresia can cause serious complications and leave mental sequelae, even leading to death.

Congenital biliary atresia is a rare disease of the liver and biliary tract that results from an unexplained inflammatory process that destroys the intrahepatic and extrahepatic bile ducts, impeding the outflow of bile. leading to fibrosis, biliary obstruction and progression of cirrhosis.

Congenital biliary atresia is a fairly rare disease of the liver and bile, appearing due to many causes such as bacterial infections, viruses, environmental factors or abnormalities in pregnancy, ...

Biliary atresia is a disease characterized by an obstruction in the flow of bile from the liver to the duodenum (small intestine), which can lead to many dangerous complications such as liver abscess, cirrhosis, liver failure or even is death. Treatment of congenital biliary atresia by surgery is an effective method to treat the disease, reducing the risk of complications.

Biliary atresia in infants is a pathology that causes cholestatic jaundice in young children, if not treated early, it can lead to bad complications such as cirrhosis, liver failure and death. The only treatment for congenital biliary atresia is surgery. Treatment after surgery with care and nutritional supplements is focused to avoid future complications for the child.

Jaundice in newborns is a manifestation of one of the diseases such as anemia, hepatitis or physiological jaundice or even congenital biliary atresia. The distinction between these diseases is to determine the direction of treatment for the child.

According to statistics, about 50-80% of newborns with congenital biliary atresia, if not treated well, will die of biliary cirrhosis when the child is 1 year old. This percentage will increase to about 90 - 100% by the time a child is 3 years old. Therefore, if the child shows signs of suspected congenital biliary atresia, the family should immediately take the child to the hospital for examination and timely diagnosis.

Congenital biliary atresia is considered a rare pathology of the liver and biliary tract, characterized by disruption or deficiency of the extrahepatic biliary system, resulting in obstruction of bile flow.

One of the major causes of cholestatic jaundice is choledochal cyst disease. This is a congenital cystic dilatation of the intra- or extrahepatic biliary system.

Congenital biliary atresia is the most common cause of biliary obstruction in nursing infants. The incidence is about 1 in 10,000 live births (1/8,000 to 1/14,000). Female/male ratio = 1:0.64.