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Updated: Jan 16, 2026

Optical Coherence Tomography: Imaging Mouse Retinal Ganglion Cells In Vivo
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带有眼运动性无力症类型2的无力症:两项血统研究和综合性审查

Lang Yang1, Sushuang Yang1, Jianfei Liu2

  • 1Department of Neurology, The Affiliated Hospital of Guizhou Medical University, Guiyang, 550004, China.

Journal of neurology
|September 30, 2025
PubMed
概括

2型眼运动性失调性缩症 (AOA2) 是一种罕见的神经退行性疾病. 这项研究确定了新的SETX突变,并发现眼运动性无力症并不总是存在的,而升高的α-fetoprotein (AFP) 是一个关键指标.

关键词:
ATAXIA与眼运动不适应性2型.临床表现 临床表现这就是SETX基因.这是一种α-fetoprotein.

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