在汉语中出现了UBQLN2基因突变的两例新病例
Shuang He1, Xin-Xin He1, Hong-Qi Yang1
1Department of Neurology, Zhengzhou University People's Hospital (Henan Provincial People's Hospital), Zhengzhou, Henan, 450003, China.
概括
罕见的UBQLN2基因变异导致X关联的主导疾病,如肌缩侧面硬化症 (ALS) 和前叶痴呆症 (FTD). 这两个汉族病例显示了UBQLN2相关疾病的显著临床多样性.
科学领域:
- 遗传学 遗传学 是一个
- 神经学 神经学
背景情况:
- UBQLN2基因的突变与X关联的主导疾病有关,包括肌缩侧面硬化症 (ALS) 和前叶痴呆症 (FTD).
- 在全球范围内,UBQLN2基因变异很少被记录,报告的病例显示出相当大的临床变异性.
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