亨廷顿病病(Huntington disease)、脊髓小脑共济失调(spinal cerebellar ataxias)、肌 萎缩侧索硬化症(amyotrophic lateral sclerosis) 及脊髓肌萎缩症(spinal muscular
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...爱问知识人 爱问知识人的观点 揪错 ┆ 评论 ┆ 举报 maybe7 [新手] 向maybe7提问 脊髓小脑共济失调（Spinocerebella Axia,SCA） 遗传性脊髓小脑性共济失调是一系列常染色体显性遗传病，病变涉及脑干和脊髓，主要病理改变是小脑和其...
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脊髓小脑共济失调2型 spinocerebellar ataxia type
型脊髓小脑共济失调 spinocerebellar ataxia type ; SCA
5型脊髓小脑共济失调 spinocerebellar ataxia type
脊髓小脑性共济失调 spinocerebellar ataxia ; SCA
脊髓小脑共济失调1型 spinocerebellar ataxia type
脊髓小脑型共济失调 spinocerebellar ataxia
性脊髓小脑性共济失调 spinocerebellar ataxia
型小脑脊髓共济失调 spino cerebell arataxiatype ; SCA
回顾小脑性共济失调的研究历史、分类，介绍脊髓小脑共济失调的病因机制和治疗方法。
The history of the research of cerebellar ataxia, and the different classifications of ataxia were reviewed. The pathogenesis and treatments of spinocerebellar ataxia were summarizd.
目的研究细胞凋亡在脊髓小脑性共济失调3型(SCA3)分子发病机制中的作用。
Objective to study the role of cell apoptosis in the molecular pathogenesis of spinocerebellar ataxia type 3 (SCA3).
目的研究遗传性脊髓小脑性共济失调7型（SCA7）的基因突变和临床特征。
Objective To study the gene mutation and clinical characteristic of hereditary spinocerebellar ataxia type 7 (SCA7).
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