Spinocerebellar Ataxia Type 2 - GeneReviews® - NCBI Bookshelf
1998年10月23日 · Spinocerebellar ataxia type 2 (SCA2) is characterized by progressive cerebellar ataxia, including nystagmus, slow saccadic eye movements, and in some …
Spinocerebellar ataxia type 2 - MedlinePlus
Spinocerebellar ataxia type 2 (SCA2) is a condition characterized by progressive problems with movement. Explore symptoms, inheritance, genetics of this condition.
什么是脊髓小脑共济失调2型？ - 知乎专栏
脊髓小脑共济失调2型 (SCA2)是中枢神经系统遗传性疾病中的一种特异性类型。 在SCA2中，遗传缺陷会导致特定的神经纤维受损，这些神经纤维传递进出大脑的信息，从而导致小脑的变性 ( …
脊髓小脑性共济失调（SCA） - 知乎 - 知乎专栏
疾病定义： 脊髓小脑 性共济失调（Spinocerebellar degeneration, SCA）也称脊髓小脑变性病，是一组具有 遗传异质性 的常染色体显性遗传神经退行性疾病，其临床特征是进行性共济失调， …
Spinocerebellar Ataxia Type 2 | Neurology Genetics
1 天前 · In SCA2, onset also frequently coincides with muscle cramping. Appendicular ataxia with instability of stance, dysarthria, and ocular signs including nystagmus and ocular dysmetria …
脊髓小脑性共济失调2型 - 中文版GeneReviews
2017年9月1日 · 脊髓小脑性共济失调 2型（Spinocerebellar ataxia type 2，SCA2）以进行性小脑性共济失调为特征，包括眼球震颤，缓慢的眼球扫视，并且在一些个体中伴有眼肌瘫痪或帕金 …
What are the symptoms of SCA2? SCA2 is very similar to SCA1 and SCA3 in that the first symptom is usually Ataxia—incoordination of the hands and trouble with balance when …
Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic ...
Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominant cerebellar ataxia that occurs as a consequence of abnormal CAG expansions in the ATXN2 gene. Progressive clinical features …
Orphanet: Spinocerebellar ataxia type 2
Spinocerebellar ataxia type 2 (SCA2) is a subtype of type I autosomal dominant cerebellar ataxia (ADCA type I; see this term) characterized by truncal ataxia, dysarthria, slowed saccades and …
Spinocerebellar ataxia 2 (SCA2) - PubMed
Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominantly inherited, neurodegenerative disease. It can manifest either with a cerebellar syndrome or as Parkinson's syndrome, while …