A Novel Mutation in the ATP7B Gene: A Rare Manifestation of Wilson Disease With Liver Failure

Wilson disease is a hereditary disorder which involves anomalous copper metabolism. Typically, the presentation is systemic, involving vital organs such as the liver, kidney, and brain, among others. We report a unique case presenting with solitary organ involvement as acute liver failure with novel...

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Detalles Bibliográficos
Autores principales: Awan, Rehmat Ullah, Rashid, Shazia, Nabeel, Ambreen, Gangwani, Manesh Kumar, Samant, Hrishikesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9911198/
https://www.ncbi.nlm.nih.gov/pubmed/36777461
http://dx.doi.org/10.14309/crj.0000000000000977

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9911198/
https://www.ncbi.nlm.nih.gov/pubmed/36777461
http://dx.doi.org/10.14309/crj.0000000000000977

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