Suppr超能文献

6型脊髓小脑共济失调(SCA 6)中的周期性交替性眼球震颤

[Periodic alternating nystagmus in spinocerebellar ataxia type 6 (SCA 6)].

作者信息

Yabe I, Sasaki H, Yamashita I, Suzuki Y, Tashiro K

机构信息

Department of Neurology, Hokkaido University School of Medicine, Sapporo, Japan.

出版信息

Rinsho Shinkeigaku. 1998 Jun;38(6):512-5.

PMID:9847668
Abstract

We report a 61-year-old man with SCA 6 manifesting periodic alternating nystagmus (PAN). He first noted transient, recurrent episodes of "dizziness" at age 56. The symptom appeared several times a day, lasting for 3 years. At age 59, unsteady gait developed insidiously. On neurological examination, he showed limb and truncal ataxia, marked gaze nystagmus, and positional nystagmus. Thereafter, his ataxia became worse and PAN developed. Brain MRI showed pathologic atrophy which was confined to the cerebellum. PAN was rarely reported in spinocerebellar ataxia, being not described in SCA 6. The episodic "dizziness" at the initial stage has not gained much attention. Our observation indicates that the initial manifestation of SCA 6 overlaps with that of episodic ataxia type 2, an allelic disorder of SCA 6. PAN and fluctuating symptoms, as seen in our patient, must be carefully examined to see whether or not they can be parts of clinical presentations in SCA 6.

摘要

我们报告了一名患有伴周期性交替性眼球震颤(PAN)的脊髓小脑共济失调6型(SCA 6)的61岁男性。他在56岁时首次注意到短暂的、反复出现的“头晕”发作。这种症状每天出现几次,持续了3年。59岁时,逐渐出现步态不稳。神经系统检查显示,他存在肢体和躯干共济失调、明显的凝视性眼球震颤和位置性眼球震颤。此后,他的共济失调加重并出现了PAN。脑部MRI显示病理性萎缩局限于小脑。PAN在脊髓小脑共济失调中很少被报道,在SCA 6中未被描述。疾病初期的发作性“头晕”并未引起太多关注。我们的观察表明,SCA 6的初始表现与发作性共济失调2型(SCA 6的等位基因疾病)的表现重叠。必须仔细检查我们患者中所见的PAN和波动症状,以确定它们是否可能是SCA 6临床表现的一部分。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验