两份RAB39B删除病例报告显示了高度可变的帕金森症
Nicolas Geoffre1, Paul Jaulent2, Chloé Laurencin2
1Lille University Hospital, Department of Toxicology and Genopathies, F-59000 Lille, France.
Parkinsonism & related disorders
|April 17, 2025
概括
韦斯曼综合征是一种罕见的遗传疾病,由RAB39B基因突变引起,导致智力障碍和帕金森症. 这项研究详细介绍了两个病例,强调了男性和女性的严重程度不同.
科学领域:
- 遗传学 遗传学 是一个
- 神经学 神经学
- 罕见疾病 罕见疾病
背景情况:
- 韦斯曼综合征是一种罕见的X系遗传疾病.
- 它与RAB39B基因的突变有关.
- 具有智力障碍和帕金森症的特征.
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