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AB160. Fuminal hepatic failure in Wilson disease
BACKGROUND: Wilson disease (WD) is an autosomal recessively inherited disorder of copper metabolism. Mutation of the ATP7B gene on chromosome 13 leads to accumulation of copper in the liver, brain, kidney and cornea. Clinical presentation is particularly in liver and central nervous system. Fuminal...
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| Publicado no: | Ann Transl Med |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
AME Publishing Company
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4563389/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3978/j.issn.2305-5839.2015.AB160 |
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