Wilson’s Disease: An Update on the Diagnostic Workup and Management
Wilson’s disease (WD) is a rare autosomal recessive disorder of hepatocellular copper deposition. The diagnostic approach to patients with WD may be challenging and is based on a complex set of clinical findings that derive from patient history, physical examination, as well as laboratory and imagin...
Enregistré dans:
Auteurs principaux: | Beata Kasztelan-Szczerbinska, Halina Cichoz-Lach |
---|---|
Format: | article |
Langue: | EN |
Publié: |
MDPI AG
2021
|
Sujets: | |
Accès en ligne: | https://doaj.org/article/4dc620ef11454037965a36cf4267bc05 |
Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|
Documents similaires
-
Chelators for Treatment of Iron and Copper Overload: Shift from Low-Molecular-Weight Compounds to Polymers
par: Martin Hruby, et autres
Publié: (2021) -
El anillo de Kayser-Fleischer como signo diagnóstico en la Enfermedad de Wilson
par: Miranda,Marcelo, et autres
Publié: (2002) -
Zinc as a Drug for Wilson’s Disease, Non-Alcoholic Liver Disease and COVID-19-Related Liver Injury
par: Pierpaolo Coni, et autres
Publié: (2021) -
Multimodal magnetic resonance imaging analysis in the characteristics of Wilson’s disease: A case report and literature review
par: Wang Yun, et autres
Publié: (2021) -
Serum Copper and Zinc in a Representative Sample of Bulgarian Population
par: Ivanova I., et autres
Publié: (2016)