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Clinical manifestations of Wilson disease in organs other than the liver and brain
Wilson disease (WD) is an inherited genetic disorder that is caused by copper metabolism disturbances with main hepatic, neurological, and psychiatric presentation. Deposits of copper accumulate in different organs and may cause a broad range of clinical manifestations. Patients with WD may present...
Guardado en:
| Publicado en: | Ann Transl Med |
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| Autores principales: | , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
AME Publishing Company
2019
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6531658/ https://ncbi.nlm.nih.gov/pubmed/31179299 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/atm.2019.03.30 |
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