脊髓小脑共济失调
表型
入射(几何)
共济失调
神经学
临床表型
医学
遗传学
突变
基因
生物
精神科
光学
物理
作者
Fengyue Han,Dan Su,Chuanqiang Qu
标识
DOI:10.1515/tnsci-2020-0190
摘要
Spinocerebellar ataxias (SCAs) are a group of neurodegenerative diseases with ataxia as the main clinical manifestation. The phenotypes, gene mutations, and involved sites of different subtypes show a high degree of heterogeneity. The incidence of SCA varies greatly among different subtypes and the case of SCA40 is extremely rare. The aim of this study is to report a rare case of SCA40 and systematically review the incidence, gene mutation, and phenotype of SCAs, especially SCA40.
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