ataxia

Neurologic symptoms of hypermagnesemia are muscular weakness, paralysis, ataxia, drowsiness, and confusion.

高镁血症的神经系统症状表现为肌肉无力 、 瘫痪 、 共济失调 、 嗜睡和意识模糊.

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Establishment of germplasm repository of spinocerebellar ataxia

脊髓小脑性共济失调遗传种质库的建立

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The Research of Clinical Features and Gene Mutation of Five Families with Spinocerebellar Ataxia in Shangdong

山东地区脊髓小脑性共济失调5个家系的临床表现和基因突变分析

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Spinocerebellar ataxia type 3/ Machado-Joseph disease ( SCA3/ MJD) is a kind of autosomal dominant disease, which is characterized by degeneration of neurons and accumulation of aberrant protein aggregates in affected neurons.

脊髓小脑型共济失调Ⅲ型/马查多-约瑟夫病（SCA3/MJD），是一种以神经细胞变性、细胞核内蛋白聚集体形成为病理特征的常染色体显性遗传病。

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Detection of trinucleotide repeat expansions in the study of hereditary spinocerebellar ataxia ( SCA) and its clinical significance

三核苷酸重复的检测在脊髓小脑型共济失调的应用研究

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Molecular Diagnostic Methods for Wilson Disease, Huntington Disease and Spinocerebellar Ataxia

肝豆状核变性、亨廷顿病和遗传性共济失调的分子诊断方法研究

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Molecular Genetic Diagnosis and Clinical Analysis of Characteristics of Spinocerebellar Ataxia Type 2

脊髓小脑性共济失调2型的分子遗传学诊断及临床分析

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Analysis of the clinical features and genetic mutation of spinocerebellar ataxia type 6 from Chinese kindreds

脊髓小脑型共济失调6型患者的临床特征及基因突变分析

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Frequency of different subtypes of spinocerebellar ataxia in the Han nationality of Hunan province in China

湖南汉族人群遗传性脊髓小脑型共济失调患者三核苷酸突变频率分布

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Ataxia cordis Atrial vulnerability and paroxysmal atrial fibrillation in canine atrium

心搏失调，心房纤维性颤动心房肌易损性与阵发性心房颤动的发生机制

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Syndrome of hemisection of the spinal cord, cerebellum ataxia.. cranial nerves sign was masculine etc.

主要临床表现有发热、乏力、头痛、呕吐、嗜睡、昏迷、抽搐、瘫痪、脊髓半切征、小脑共济失调、颅神经征阳性等。

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On the basis of animal experiment, 9~ 12 week human embryonic cerebellar tissue suspension was transplanted into the cerebellum of 6 medically intractable patients with severe hereditary cerebellar degenerative ataxia.

在动物实验基础上，将胎龄为9～12周的人胚胎小脑组织悬液移植到6例患有严重小脑萎缩的患者脑内。

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ObjectiveTo investigate the efficacy of acupuncture in ataxia cerebral palsy.

目的探讨针刺疗法治疗共济失调型脑瘫的疗效.

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Objective To study the role of cell apoptosis in the molecular pathogenesis of spinocerebellar ataxia type 3 ( SCA3).

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。

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Frequency analysis of autosomal dominant spinocerebellar ataxias in Han population in the Chinese mainland and clinical and molecular characterization of spinocerebellar ataxia type 6

中国大陆汉族人群SCA各亚型的突变频率分析及SCA6的临床和分子特征

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Since the identification of the first gene responsible for spinocerebellar ataxia type 1 ( SCA1) in 1993, an increasing number of genes and chromosomal loci have been characterized.

自从1993年，第一个SCA亚型（SCA1）被鉴定以来，不断有新的位点被发现，到目前为止至少发现有27种SCA亚型。

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The Clinical Features and Molecular Biology Studies on Hereditary Spinocerebellar Ataxia Type 3 in Ningxia Area

宁夏地区遗传性脊髓小脑性共济失调3型的临床与分子研究

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Other possible symptoms are ataxia, vertigo, seizures, and dysphagia.

其他可能的症状还有共济失调 、 眩晕 、 癫痫发作和吞咽困难.

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The victim then experiences a tingling sensation in the mouth and extremities, double vision, tunnel vision, severe confusion, fever, excessive salivation ( including foaming of the mouth and nose) and pronounced ataxia ( lack of muscle control).

然后中毒者会出现嘴和四肢发麻、复视、管状视、严重神经错乱、发烧、过度流涎症（包括嘴和鼻子起泡）和明显的共济失调（因肌肉停止运作而发生）。

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The clinical features of the spinocerebellar ataxia include ataxa, dysarthria, dysmetria et al. The gene diagnosis can be used as diagnostic criteria and the detection of repeats times of CAG can provide an effective way for the genetic and presymptomatic diagnosis.

临床特征有共济失调、构音障碍，基因诊断是一种准确的诊断方法和标准，CAG重复序列数目的检测对于基因诊断和症状前诊断是一种十分有效的方法。

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Minimum prevalence of spinocerebellar ataxia 17 in the north east of England

英格兰东北部17型脊髓小脑性共济失调的最低患病率

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We diagnosised 2 spinocerebellar ataxia type 3 pedigrees, including 20 familial patients, for the first time in the Three Gorge Reservoir Area. 3.

三峡库区首次确诊2个脊髓小脑性共济失调3型家系，其中有20名家系患者。

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Analysis of the gene mutation and clinical characteristic of hereditary spinocerebellar ataxia type 7

遗传性脊髓小脑性共济失调7型的基因突变及临床特征分析

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We diagnosised 1 sporadic patients of spinocerebellar ataxia type 3 for the first time in the Three Gorge Reservoir Area. 4.

三峡库区首次确诊1名脊髓小脑性共济失调3型散发患者。

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These signs are followed by ataxia.

这些症状之后就是共济失调.

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Conclusion: The point mutation in this area of mitochondrial DNA might not be related hereditary ataxia.

结论: 遗传性共济失调的发生、发展可能与该区域点突变无关.

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Objective To explore SCA 3 gene mutation in the patients with inherited spinocerebellar ataxia.

1目的探讨遗传性脊髓小脑型共济失调（SCA）病人SCA3基因突变的意义。

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The typical clinical manifestations were vertigo, cerebellar ataxia as well as nystagmus.

临床表现以眩晕、呕吐 、 小脑性共济失调、眼球震颤为主.

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Objective To study the clinical features and genetic mutation frequency of spinocerebellar ataxia ( SCA) type 6 from Chinese kindreds.

目的研究脊髓小脑型共济失调（SCA）6型的临床特征和基因突变频率。

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Objective : To study the possible relationship between mitochondrial DNA point mutations and hereditary ataxia.

目的: 探索线粒体DNA点突变与遗传性共济失调的关系.

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