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Late onset fulminant Wilson’s disease: A case report and review of the literature
Wilson’s disease (WD) is an autosomal recessive inherited disorder of hepatic copper metabolism. WD can be present in different clinical conditions, with the most common ones being liver disease and neuropsychiatric disturbances. Most cases present symptoms at < 40 years of age. However, few repo...
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| Publicado no: | World J Gastroenterol |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Baishideng Publishing Group Inc
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4265628/ https://ncbi.nlm.nih.gov/pubmed/25516681 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3748/wjg.v20.i46.17656 |
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