在泛性 dystonia 新的 de novo 异构体 CACNA1A 基因变异: 一个案例报告

Mohammed Alshareet1, Aljoharah Alakkas2, Omar A Alsinaidi2

  • 1Department of Neurology, National Neuroscience Institute, KFMC, Riyadh, Saudi Arabia.

BMJ neurology open
|June 24, 2024
PubMed
概括

在一个患有 dystonia 的年轻人身上发现了一种罕见的 CACNA1A 基因变异,呈现出运动障碍症状. 这一发现表明,当其他遗传检测结果为阴性时,CACNA1A基因测试可用于 dystonia.

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