Infants with biliary atresia usually appear healthy at birth. Most often, symptoms develop within the first two weeks to two months of life. The majority of children with jaundice undergo a series of tests to distinguish biliary atresia from other conditions.
Your doctor will perform a physical exam and will look for or ask questions about the following: jaundice; dark urine; light or pale colored stools; distended abdomen; poor weight gain.
A variety of blood tests can be used to assess liver function. They include:
Tests may also be done on urine and stool to detect infection and the amount of bilirubin and bilirubin by-products present. Jaundice and other symptoms noted with biliary atresia may also be seen in children with cystic fibrosis. A test that measures the amount of chloride present in a baby's sweat may be done to determine if the child actually has cystic fibrosis.
A tissue sample is taken from your child's liver and examined for abnormalities, allowing biliary atresia to be distinguished from other liver problems.
In some cases, a cholangiogram is performed in the operating room. This is an x-ray imagining study performed by a surgeon in the operating room to determine whether any of the bile ducts are open either outside or inside the liver. This test is used to determine the cause of obstructed bile flow.