与CACNA1A突变相关的偏头痛与延长的非相性光环:一个病例报告和叙事审查
Crystal J Jicha1, Ashley Alex2, Steven Herskovitz3
1Department of Neurology, University of California Irvine, Irvine, California, USA.
Headache
|June 27, 2023
概括
一种CACNA1A基因变异与长时间的无半的非相性光环有关,扩大了已知的家族半性偏头痛 (FHM) 谱. 这一发现有助于诊断罕见的神经疾病,包括失语症和遗传突变.
科学领域:
- 遗传学 遗传学 是一个
- 神经学 神经学
背景情况:
- 长期失言症没有半的差异诊断包括血管疾病,发作,代谢问题和偏头痛.
- CACNA1A基因突变与家族性半性偏头痛 (FHM) 类型1有关,呈现出单侧弱气.
- 之前没有报告与CACNA1A突变相关的无半衰症的失语症.
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