Spinocerebellar ataxia type 3 with dopamine-responsive dystonia: A case report

BACKGROUND: Spinocerebellar ataxia type 3 (SCA3) is a rare neurodegenerative disease with high genetic heterogeneity. SCA3 mainly manifests as progressive cerebellar ataxia accompanied by paralysis of extraocular muscles, dysphagia, lingual fibrillation, pyramidal tract sign, and extrapyramidal syst...

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Detalles Bibliográficos
Autores principales: Zhang, Xiao-Le, Li, Xiao-Bo, Cheng, Fa-Feng, Liu, Shu-Ling, Ni, Wen-Chao, Tang, Fei-Fei, Wang, Qing-Guo, Wang, Xue-Qian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8554412/
https://www.ncbi.nlm.nih.gov/pubmed/34754867
http://dx.doi.org/10.12998/wjcc.v9.i28.8552

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