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共济失调

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The neurological abnormalities can be classifi ed as: an akinetic-rigid syndrome similar to Parkinson's disease, pseudosclerosis dominated by tremor, ataxia, and a dystonic syndrome.

神经系统的异常可以分为以下几类:a 类似于帕金森氏病的运动不能-肌强直综合征;b以震颤为主要表现的假性多发性硬化;c共济失调; d 肌张力障碍综合征。

Progressive supranuclear palsy is a degenerative neurological disorder of uncertain etiology characterized by gait ataxia, slowing or inability to generate voluntary saccadic eye movements, and axial rigidity.

译:进行性核上性麻痹是病因不明的神经系统退行性病变,临床表现为共济失调步态、自主眼球扫视运动无法完成或完成缓慢、躯干强直。

The authors describe the case of a 45-year-old man with progressive gait ataxia and sensorimotor deficits of the upper and lower extremities.

作者描述了一例45岁男性渐进性的步态共济失调和手足感觉运动缺陷患者。

Objective To study the gene mutation characteristics of patients with spinocerebellar ataxias in Ningxia region.

目的 研究宁夏地区脊髓小脑性共济失调患者基因突变的特征。

Objective To determine the frequency of different subtypes of spinocerebellar ataxias in the Han nationality of Hunan province in China.

目的:研究湖南汉族人群中脊髓小脑性共济失调不同基因亚型的分布状况。

Spinocerebellar ataxias are a group of autosomal dominant cerebellar degenerative disorders, which are characterized by clinical and genetic variability.

脊髓小脑性共济失调是一组常染色体显性的小脑退行性病,具有临床和遗传多样性。

We investigated the clinical features and gene mutation in a pedigree of spinocerebellar ataxia.

对一脊髓小脑性共济失调(Spinocerebenllar ataxia, SCA)家系的患者进行临床特征及相关基因突变研究。

Spinocerebellar ataxia type 7 (SCA7) is less variable in clinical presentation than other SCAs.

脊髓小脑性共济失调7型(SCA7)的临床表现形式较其它SCA类型少。

Ataxin-1 is another pathogenic protein which causes a disease called spinocerebellar ataxia, which is also an incurable hereditary nervous disorder.

Ataxin-1是另一种致病蛋白,它能够引起脊髓小脑性共济失调,也是一种不能治愈的遗传性神经系统疾病。

Objective To screen for proteins interacting with ataxin-3 by yeast two-hybrid system 3, and to discuss the function of ataxin-3 and pathogenesis of spinocerebellar ataxia type 3 and Machado-Joseph disease (SCA3/MJD).

目的:利用酵母双杂交系统3筛选与ataxin-3相互作用的蛋白质,探讨ataxin-3的功能和脊髓小脑型共济失调Ⅲ型(SCA3/MJD)的发病机制。

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