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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Shranjeno v:
Bibliografske podrobnosti
izdano v:Case Rep Med
Main Authors: Bekele, Nebiyu, Ewnetu, Frew, Hailu, Tigest, Tegegne, Zerubabel, Tadesse, Abilo
Format: Artigo
Jezik:Inglês
Izdano: Hindawi 2020
Teme:
Case Report
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC7396006/
https://ncbi.nlm.nih.gov/pubmed/32774387
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2020/7650170
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