Wilson's Disease: Diagnosis of Wilson's Disease in Ethiopian Young Sisters

BACKGROUND: Wilson's disease is an inherited autosomal recessive disorder of copper metabolism. Clinical signs, biochemical parameters, histologic findings, and/or ATP7B genetic testing are required to diagnose Wilson's disease. Case Presentation. 25-year-old and 22-year-old young women (s...

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Detalles Bibliográficos
Autores principales: Bekele, Nebiyu, Ewnetu, Frew, Hailu, Tigest, Tegegne, Zerubabel, Tadesse, Abilo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7396006/
https://www.ncbi.nlm.nih.gov/pubmed/32774387
http://dx.doi.org/10.1155/2020/7650170

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7396006/
https://www.ncbi.nlm.nih.gov/pubmed/32774387
http://dx.doi.org/10.1155/2020/7650170

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