Dystonia as a presenting sign of spinocerebellar ataxia type 1
Dystonia as a presenting sign of spinocerebellar ataxia type 1
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DOI：
10.1002/mds.10708
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发表时间：
2004-05-01
影响因子：
8.6
通讯作者：
Chen, ST
中科院分区：
文献类型：
--
作者：
Wu, YR;Lee-Chen, GJ;Chen, ST
我们报告一位39岁男性，最初表现为眼睑痉挛，口下颌肌张力障碍和后倾，一年后发展为轻度共济失调。我们的研究结果表明，肌张力障碍可能是SCA1的致残性表现，并支持SCA1的临床异质性，强调了在肌张力障碍和小脑共济失调患者中考虑该实体的重要性。(C)2003年，为社会运动员。
We report on a 39-year-old man who presented initially with marked blepharospasm, oromandibular dystonia and retrocollis and one year later developed mild ataxia. Our findings suggest that dystonia can be it disabling presenting sign of SCA1 and support the clinical heterogeneity of SCA1, highlighting the importance of considering this entity in patients combining dystonia and cerebellar ataxia. (C) 2003 Movement Disorder Society.