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Aetiology of biliary atresia: what is actually known?
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 bee...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3766137/ https://www.ncbi.nlm.nih.gov/pubmed/23987231 http://dx.doi.org/10.1186/1750-1172-8-128 |
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author | Petersen, Claus Davenport, Mark |
author_facet | Petersen, Claus Davenport, Mark |
author_sort | Petersen, Claus |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-3766137 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-37661372013-09-08 Aetiology of biliary atresia: what is actually known? Petersen, Claus Davenport, Mark Orphanet J Rare Dis Review 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. BioMed Central 2013-08-29 /pmc/articles/PMC3766137/ /pubmed/23987231 http://dx.doi.org/10.1186/1750-1172-8-128 Text en Copyright © 2013 Petersen and Davenport; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Petersen, Claus Davenport, Mark Aetiology of biliary atresia: what is actually known? |
title | Aetiology of biliary atresia: what is actually known? |
title_full | Aetiology of biliary atresia: what is actually known? |
title_fullStr | Aetiology of biliary atresia: what is actually known? |
title_full_unstemmed | Aetiology of biliary atresia: what is actually known? |
title_short | Aetiology of biliary atresia: what is actually known? |
title_sort | aetiology of biliary atresia: what is actually known? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3766137/ https://www.ncbi.nlm.nih.gov/pubmed/23987231 http://dx.doi.org/10.1186/1750-1172-8-128 |
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