[脊髓小脑共济失调 2 以下运动神经元受累为首发症状:病例报告]。

Q4 Medicine
Clinical Neurology Pub Date : 2024-01-20 Epub Date: 2023-12-08 DOI:10.5692/clinicalneurol.cn-001910
Manami Matsushita, Yoshitsugu Nakamura, Takafumi Hosokawa, Yuji Takahashi, Hidehiro Mizusawa, Shigeki Arawaka
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引用次数: 0

摘要

一名 36 岁的男子出现左手拇指无力、左侧耳廓肌和左侧第一背侧骨间肌萎缩的症状已有一年,但无感觉障碍。神经传导检查显示复合肌肉动作电位振幅下降,左内侧神经出现 F 波。针刺肌电图检查显示,左侧外展肌的尖波呈阳性,运动单位后来被招募。脑磁共振成像显示双侧小脑半球萎缩。他的祖母和两个叔叔被诊断为脊髓小脑变性。出院后,他出现了双下肢共济失调。基因分析表明,ATXN2 基因中存在杂合的 CAG 重复扩增(19/39),被诊断为脊髓小脑共济失调 2(SCA2)。之前的一份报告显示,在同一血统中,ATXN2 基因全 CAG 重复扩增的患者运动神经元受累被认为是 SCA2 的一部分。我们在此报告了一名以下运动神经元受累作为 SCA2 最初症状的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Spinocerebellar ataxia 2 develop lower motor neuron involvement as an initial symptom: a case report].

A 36-year-old man has developed weakness of left thumb and atrophy of left thenar muscle and left first dorsal interosseous muscle without sensory disturbance for a year. A nerve conduction study revealed decreases in the amplitude of compound muscle action potentials and occurrence of F-waves on left medial nerve. Needle electromyography examination revealed positive sharp waves and later recruited motor units on left abductor pollicis brevis muscle. Brain MRI showed atrophy of bilateral cerebellar hemisphere. His grandmother and his two uncles have been diagnosed as spinocerebellar degeneration. After discharge, he developed bilateral lower limb ataxia. Genetic analysis showed heterozygous CAG repeat expansion (19/39) in ATXN2 gene, being diagnosed as spinocerebellar ataxia 2 (SCA2). A previous report has shown that motor neuron involvement is recognized as part of SCA2 in the same pedigree with full CAG repeat expansions in ATXN2 gene. We here report the patient with lower motor neuron involvement as an initial symptom of SCA2.

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来源期刊
Clinical Neurology
Clinical Neurology Medicine-Neurology (clinical)
CiteScore
0.30
自引率
0.00%
发文量
147
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