Eye Involvement in Wilson’s Disease: A Review of the Literature

Wilson’s disease (WD) is an autosomal recessive genetic disorder due to a mutation of the ATP7B gene, resulting in impaired hepatic copper excretion and accumulation in various tissues. Ocular findings are one of the hallmarks of the disease. Many ophthalmological manifestations have been described...

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Detalles Bibliográficos
Autores principales: Chevalier, Kevin, Mauget-Faÿsse, Martine, Vasseur, Vivien, Azar, Georges, Obadia, Michaël Alexandre, Poujois, Aurélia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9102176/
https://www.ncbi.nlm.nih.gov/pubmed/35566651
http://dx.doi.org/10.3390/jcm11092528

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9102176/
https://www.ncbi.nlm.nih.gov/pubmed/35566651
http://dx.doi.org/10.3390/jcm11092528

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