与非典型的多重系统缩样表型相关的异构基APTX突变:一个病例报告
Alberto Imarisio1, Andrea Pilotto2, Alessandro Lupini3
1Department of Molecular Medicine, University of Pavia, Pavia, Italy; IRCCS Mondino Foundation, Pavia, Italy.
Parkinsonism & related disorders
|March 31, 2024
概括
罕见的APTX基因突变,通常会导致1型眼运动无力症的动脉缩,可能会影响多系统缩帕金森症 (MSA-P) 风险和73岁患者的呈现.
科学领域:
- 神经遗传学 神经遗传学
- 神经退行性疾病 神经退行性疾病
- 缺氧综合征 缺氧综合征
背景情况:
- 多系统缩帕金森症 (MSA-P) 是一种罕见的神经退行性疾病.
- 带有眼运动不良反应类型1 (AOA1) 的动性通常是由APTX基因中的同卵性突变引起的.
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