Quality of life and depression in Wilson’s disease: a large prospective cross-sectional study

BACKGROUND: 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. Lifelong decoppering treatments are the keystone of the treatment. These treatments can prevent,...

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Detalles Bibliográficos
Autores principales: Chevalier, Kevin, Rahli, Djamila, de Veyrac, Louise, Guillaume, Jessica, Obadia, Michaël Alexandre, Poujois, Aurélia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10308610/
https://www.ncbi.nlm.nih.gov/pubmed/37386576
http://dx.doi.org/10.1186/s13023-023-02777-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10308610/
https://www.ncbi.nlm.nih.gov/pubmed/37386576
http://dx.doi.org/10.1186/s13023-023-02777-4

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