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 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.

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.

Jaundice due to increased direct bilirubin is one of the common causes of jaundice in newborns. To avoid dangerous complications, it is necessary to clearly understand the causes and treatment methods of jaundice due to increased direct bilirubin in the early stages.

Congenital biliary atresia in children is a dangerous disease that needs to be treated early. Surgery is the optimal treatment method today. After surgery, the child needs careful care to avoid biliary tract infection and increased portal vein pressure.

Hepatobiliary diseases in children are caused by many different diseases, the most common of which is congenital biliary atresia. Early detection and treatment of hepatobiliary diseases in children will improve treatment effectiveness and avoid leaving serious sequelae.

Biliary atresia is a congenital condition that causes impaired liver function and leads to cirrhosis. It is a complex disease with an unclear etiology. Observations suggest that the incidence of the disease is higher in regions and ethnicities such as Southeast Asia and the South Pacific Islands.