IF 1.9 Q3 CLINICAL NEUROLOGY
Georges-Junior Kahwagi , Cécile Hubsch , Lydie Burglen , Jean-Philippe Brandel , Sophie Sangla , Clément Desjardins
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引用次数: 0

摘要

我们报告了一种成人发病的与 KMT2B 相关的肌张力障碍,其演变过程分为两个阶段:局灶性颈椎发病,随后迅速泛化。全基因组测序确定了一个可能致病的 KMT2B 变体。双苍白球深部脑刺激疗法使患者的运动能力提高了83%,凸显了该疗法对晚期发病的非典型两阶段演变型KMT2B肌张力障碍的治疗潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bi-pallidal deep brain stimulation as an effective therapy in atypical two-stage evolution adult-onset KMT2B-related dystonia
We report an adult-onset KMT2B-related dystonia with a two-stage evolution: focal cervical onset followed by rapid generalization. Whole genome sequencing identified a likely pathogenic KMT2B variant. Bi-pallidal deep brain stimulation led to an 83% motor improvement, highlighting its therapeutic potential in late-onset atypical two-stage evolution KMT2B-dystonia.
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来源期刊
Clinical Parkinsonism  Related Disorders
Clinical Parkinsonism Related Disorders Medicine-Neurology (clinical)
CiteScore
2.70
自引率
0.00%
发文量
50
审稿时长
98 days
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