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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...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Wolters Kluwer
2023
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| Materias: | |
| 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 |