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Spinocerebellar ataxia 2 presenting as Parkinsonism: two families report and literatures review

Objective To summarize the clinical, imaging and genetic characteristics of spinocerebellar ataxia 2 (SCA2) families presenting as Parkinsonism. Methods and Results Two families with autosomal dominant SCA2 with Parkinson's syndrome diagnosed by genetic test in Peking University First Hospital from...

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Principais autores: WAN Ya⁃lan, JIANG Yan⁃yan, ZHOU Hong, ZHENG Yi⁃ming, LÜ He, ZHAO Gui⁃ping, CHEN Jing, SUN Wei, WANG Zhao⁃xia
Formato: Artigo
Idioma:Inglês
Publicado em: Tianjin Huanhu Hospital 2022-08-01
coleção:Chinese Journal of Contemporary Neurology and Neurosurgery
Assuntos:
spinocerebellar ataxias
parkinsonian disorders
genes
mutation
trinucleotide repeat expansion
pedigree
Acesso em linha:http://www.cjcnn.org/index.php/cjcnn/article/view/2553
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