Generalized Dystonia as Presenting Feature of Wilson Disease: A Case Report

Wilson disease is a rare autosomal recessive genetic disease, caused by the mutation of the ATP7B gene leading to decreased secretion of serum ceruloplasmin in blood and decrease biliary excretion of copper leading to toxic level accumulation in the liver, brain, kidney, and cornea, resulting in dev...

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Detalles Bibliográficos
Autores principales: Anushree, Akansha, Kumar, Sudesh, Bhattacharya, Piyali, Tripathi, Siddharth, Chattopadhyay, Nandita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10041581/
https://www.ncbi.nlm.nih.gov/pubmed/36992844
http://dx.doi.org/10.1177/2333794X231163418

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10041581/
https://www.ncbi.nlm.nih.gov/pubmed/36992844
http://dx.doi.org/10.1177/2333794X231163418

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