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Wilson disease with hepatic presentation in an eight-month-old boy
Wilson disease is an autosomal recessive disorder of copper metabolism that can cause fatal neurological and hepatic disease if not diagnosed and treated. The youngest child with normal liver function reported so far is an 8-mo-old Japanese boy with low ceruloplasmin levels, and the youngest child w...
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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
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4528042/ https://ncbi.nlm.nih.gov/pubmed/26269689 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3748/wjg.v21.i29.8981 |
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