Neurologic Wilson disease: case series on a diagnostic and therapeutic emergency

Wilson disease is a rare genetic disease causing pathologic deposition of copper in the liver, brain, cornea, kidney, and cardiac muscles. Presented are two cases of neurologic Wilson disease with progressive movement disorder and Kayser-Fleischer rings with low serum copper, low ceruloplasmin, and...

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Detalles Bibliográficos
Autores principales: Porlas Jr, Romeo V., de Castillo, Lennie Lynn C., Dioquino, Carissa Paz C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Les Laboratoires Servier 2018
Materias:
Free Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6436958/
https://www.ncbi.nlm.nih.gov/pubmed/30936772

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6436958/
https://www.ncbi.nlm.nih.gov/pubmed/30936772

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