| 遗传性小脑型共济失调症(附55例报告) |
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| 引用本文： | 徐越,牟琪琪.遗传性小脑型共济失调症(附55例报告)[J].重庆医学,1986(4). |
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| 作者姓名： | 徐越 牟琪琪 |
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| 作者单位： | 重庆医科大学神经病学教研室
(徐越)，重庆医科大学神经病学教研室(牟琪琪) |
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| 摘 要： | 本文分析了55例小脑型遗传性共济失调的临床资料，男女之比为4：1，2/3患者年龄在37～50之间，并发症状多为行走不稳。主要临床表现为兼有躯干和肢体共济失调（78.2％），眼震（56.4），构音障碍（69.l％），约1/4病人有病理征及家族史。讨论了本病与其他疾病所致共济失调的鉴别诊断，以及本病的病理学基础。
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| 关 键 词： | 共济失调 小脑型 遗传性 |
HEREDIFARY CEREBELLAR ATAXIA |
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| Xlu Yue,et al..HEREDIFARY CEREBELLAR ATAXIA[J].Chongqing Medical Journal,1986(4). |
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| Authors: | Xlu Yue |
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| Affiliation: | Xlu Yue,et al.First Hospital of Chongqing Medical University,Chongqing |
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| Abstract: | 55 cases of hereditary cerebellar ataxia were analysed. Males were 4 times as many as females, Two-thirds of the patients were in the ages between 31 and 50. The majority of the inifial symptoms were unstable gait. The chief clinical symptoms were truacal ataxia and limb ataxia (78.2%), nystagmus (56.4%). dysarthria (69.1%). About a quarter of the patients had positive Babinski's sign and a family history. The differential diagnosis between hereditary cerebellar ataxia and other systemic disorders were discussed, and pathological basis of this disease was described. |
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| Keywords: | Ataxia Cerebellar Hereditary |
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