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Management Perspective of Wilson’s Disease: Early Diagnosis and Individualized Therapy

Wilson’s disease (WD) is an inherited disease caused by mutations in ATP7B and is characterized by the pathological accumulation of copper in the liver and brain. Common clinical manifestations of WD include a wide range of liver disease and neurological symptoms. In some patients, psychiatric sympt...

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Detalhes bibliográficos
Publicado no:Curr Neuropharmacol
Main Authors: Yuan, Xiang-Zhen, Yang, Ren-Min, Wang, Xiao-Ping
Formato: Artigo
Idioma:Inglês
Publicado em: Bentham Science Publishers 2021
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8206458/
https://ncbi.nlm.nih.gov/pubmed/32351182
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2174/1570159X18666200429233517
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