肌阵挛-肌张力障碍的步态障碍(DYT-SGCE)

IF 2.5 Q2 CLINICAL NEUROLOGY
G. Haeri, G. Shahidi, A. Fasano, M. Rohani
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引用次数: 0

摘要

背景肌阵挛-肌张力障碍通常表现为肌阵挛和肌张力障碍的可变组合,主要累及颈部和手臂,但累及腿部,尤其是作为首发症状,并不常见。病例报告一名29岁的Epsilon-sarcoglycan (SGCE)基因杂合突变的女性表现为右腿快速抽搐,干扰行走。她还表现出张力障碍姿势和躯干和上肢近端抽搐。虽然不典型,但累及腿部可能是肌阵挛-肌张力障碍的表现,无论是在首发时还是在疾病进展过程中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gait Impairment in Myoclonus–Dystonia (DYT-SGCE)
Background Myoclonus–dystonia usually presents variable combination of myoclonus and dystonia mainly affecting the neck and arms, but leg involvement, especially as the presenting sign, is not common. Case report A 29-year-old lady with a heterozygous mutation in Epsilon-sarcoglycan (SGCE) gene is presented with rapid jerks of the right leg interfering with walking. She has also manifested dystonic posture and jerks of the trunk and proximal upper limbs. Discussion Although it is not typical, leg involvement could be a manifestation of myoclonus–dystonia either at presentation or during disease progression.
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来源期刊
CiteScore
4.00
自引率
4.50%
发文量
31
审稿时长
6 weeks
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