Biliary Atresia is a rare liver condition that affects newborns. It occurs when the bile ducts, which help carry bile from the liver to the gallbladder and intestines, are blocked or absent. This blockage prevents bile from flowing properly, leading to liver damage and jaundice, a yellowing of the skin and eyes. If not treated early, Biliary Atresia can cause serious health issues. The most common treatment is a surgical procedure called the Kasai procedure, which helps restore bile flow. In some cases, a liver transplant may be necessary to ensure the child’s long-term health and well-being.