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6型脊髓小脑共济失调中的眩晕和前庭异常

Vertigo and vestibular abnormalities in spinocerebellar ataxia type 6.

作者信息

Yu-Wai-Man Patrick, Gorman Grainne, Bateman David E, Leigh R John, Chinnery Patrick F

机构信息

Mitochondrial Research Group, School of Neurology, Neurobiology and Psychiatry, The Medical School, Newcastle University, Newcastle upon Tyne, NE2 4HH, UK.

出版信息

J Neurol. 2009 Jan;256(1):78-82. doi: 10.1007/s00415-009-0068-2. Epub 2009 Feb 9.

Abstract

Spinocerebellar ataxia type 6 (SCA6) is a calcium channelopathy due to a pathological CAG repeat expansion in CACNL1A4. Patients frequently describe paroxysmal vertigo early in the disease course, but it is not clear whether this is central or labyrinthine in origin. To address this issue we studied 21 SCA6 patients. Symptoms of vertigo were defined using a structured questionnaire. Signs were recorded during a standardised bed-side vestibular examination that included systematic positional testing with Frenzel goggles.Brief, recurrent attacks of vertigo occurred in 13 patients, usually preceding the onset of ataxia. Nystagmus was observed behind Frenzel goggles in 14 patients, and was induced either during positional testing, or head shaking in 20 patients. Only one patient had findings typical of benign paroxysmal positional vertigo (BPPV). Combined downbeat and horizontal gaze-evoked nystagmus ("side-pocket") was the most common form, occurring most commonly in supine and head-hanging positions, and following horizontal head-shaking. Nystagmus beating away from the ground (apogeotropic) occurred in 9 patients as they lay on their side.In conclusion, vertigo and abnormalities on bedside vestibular examination are common in SCA6, with forms of nystagmus typical of cerebellar, rather than labyrinthine, disease. These findings demonstrate phenotypic overlap between SCA6 and episodic ataxia type 2, which are both due to mutations in CACNL1A4.

摘要

6型脊髓小脑共济失调(SCA6)是一种钙通道病,由CACNL1A4基因中病理性的CAG重复序列扩增所致。患者在病程早期常描述有阵发性眩晕,但尚不清楚其起源是中枢性还是迷路性。为解决这一问题,我们研究了21例SCA6患者。使用结构化问卷对眩晕症状进行定义。在标准化床边前庭检查过程中记录体征,该检查包括使用Frenzel眼镜进行系统的位置测试。13例患者出现短暂、反复发作的眩晕,通常在共济失调发作之前。14例患者在Frenzel眼镜后观察到眼球震颤,其中20例患者在位置测试或摇头时诱发眼球震颤。只有1例患者有典型的良性阵发性位置性眩晕(BPPV)表现。下跳性和水平性凝视诱发眼球震颤(“侧袋”)合并出现是最常见的形式,最常出现在仰卧位和头悬垂位,以及水平摇头后。9例患者侧卧时出现背离地面的眼球震颤(离地性)。总之,眩晕和床边前庭检查异常在SCA6中很常见,眼球震颤形式为小脑疾病而非迷路疾病所特有。这些发现表明SCA6与2型发作性共济失调之间存在表型重叠,二者均由CACNL1A4基因突变引起。

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