在患有异卵性SQSTM1变体的患者中呈现出非典型的眼睛肌痛症样表现
Milaris M Sanchez-Cordero1, Josean M Rosado1, Felix Rivera Troia1
1Internal Medicine, Mayaguez Medical Center, Mayaguez, PRI.
Cureus
|August 7, 2025
概括
一名患有不明原因视力和肌肉症状的患者被诊断出患有罕见的SQSTM1基因变异. 这一发现扩大了对神经肌肉疾病的理解,并突出了基因测试的重要性.
科学领域:
- 神经学 神经学
- 遗传学 遗传学 是一个
- 分子生物学分子生物学
背景情况:
- 神经肌肉结合障碍可以表现为各种症状,包括双眼视,死和视力模糊.
- 血清阴性疾病由于缺乏特定的自身抗体而带来诊断挑战.
关键词:
基因检测 基因检测是指基因检测.神经肌肉结合障碍 神经肌肉结合障碍眼部骨髓缩症 眼部骨髓缩症 眼部骨髓缩症重复的神经刺激是重复的神经刺激.血清消极的严重肌痛性肌痛症.这就是Sqstm1的意思.更多相关视频
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