Endocrine Symptoms as the Initial Manifestation of Wilson’s Disease

Wilson’s disease is a rare genetic disorder of copper metabolism. The difference in copper tissue accumulation is responsible for the various clinical manifestations of this disorder. If left untreated, Wilson’s disease progresses to hepatic failure, severe neurological disability, and even death. D...

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Detalles Bibliográficos
Autores principales: Krysiak, Robert, Handzlik-Orlik, Gabriela, Okopien, Boguslaw
Formato: Online Artículo Texto
Lenguaje:English
Publicado: YJBM 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3375662/
https://www.ncbi.nlm.nih.gov/pubmed/22737053

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3375662/
https://www.ncbi.nlm.nih.gov/pubmed/22737053

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