Biliary atresia (BA) is a rare disease of unknown etiology and unpredictable outcome, even when there has been timely diagnosis and exemplary surgery. It has been the commonest indication for liver transplantation during childhood for the past 20 years. Hence much clinical and basic research has been directed at elucidating the origin and pathology of BA. This review summarizes the current clinical variations of BA in humans, its occasional appearance in animals and its various manifestations in the laboratory as an experimental model. © 2013 Petersen and Davenport; licensee BioMed Central Ltd.
CITATION STYLE
Petersen, C., & Davenport, M. (2013). Aetiology of biliary atresia: What is actually known? Orphanet Journal of Rare Diseases. https://doi.org/10.1186/1750-1172-8-128
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