遗传确认的Charcot-Marie-Tooth病2A型表现为姿势震:一个病例报告
Salhadin Mohammed1, Selam Kifelew2, Fikru Tsehayneh2
1Department of Internal Medicine, Neurology Unit, Wollo University, PO. Box 26901, Dessie, Ethiopia. salhadinm50@gmail.com.
Journal of medical case reports
|November 28, 2024
概括
这项案例研究突出了34岁男性患有神经病态姿势震的Charcot-Marie-Tooth疾病亚型2A的罕见表现. 这些发现强调了在诊断外围神经病变时考虑震的重要性.
科学领域:
- 神经学 神经学
- 遗传学 遗传学 是一个
- 周围神经病变是一种神经病变.
背景情况:
- 查尔科-玛丽-牙病 (CMT) 是一组遗传的神经系统疾病,导致渐进的肌肉衰弱和感官丧失.
- 姿势震是CMT中不常见的症状,通常与罗西-莱维综合征 (CMT类型1) 相关.
- 诊断CMT与震可能是具有挑战性的,因为它是罕见的.
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