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Central pontine myelinolysis associated with Wilson disease in a 7-year-old child
Wilson disease is a rare heredodegenerative inborn error of copper metabolism with varied neuropsychiatric, hepatic and other manifestations. Here we report a case of Wilson disease with neurological manifestations in a 7-year-old girl with concurrent asymptomatic liver involvement and characteristi...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Publishing Group
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3670078/ https://ncbi.nlm.nih.gov/pubmed/23704419 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2012-007408 |
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