Abstract
Biliary atresia is a serious condition affecting bile drainage from the liver to the small intestine caused by a progressive fibro-proliferative obliteration of the extrahepatic bile ducts. Untreated, it can lead to progressive liver failure, cirrhosis, and death. Broadly two types of biliary atresia exist, acquired and fetal. Infants with persistent jaundice or acholic stools beyond 3 weeks of life should be evaluated for biliary atresia. Definitive treatment requires Kasai portoenterostomy or liver transplantation. Biliary atresia requires a methodical and multidisciplinary diagnostic workup and treatment plan.
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Lillegard, J.B., Miller, A.C., Flake, A.W. (2017). Biliary Atresia. In: Mattei, P., Nichol, P., Rollins, II, M., Muratore, C. (eds) Fundamentals of Pediatric Surgery. Springer, Cham. https://doi.org/10.1007/978-3-319-27443-0_78
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DOI: https://doi.org/10.1007/978-3-319-27443-0_78
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