一个罕见的Desmin和ThioredoxinReductase 2基因同时发生突变的案例,导致扩展性心肌病
Nazima Khatun1, Sahil Zaveri1, Louis Salciccioli2
1Internal Medicine, State University of New York Downstate Medical Center, Brooklyn, USA.
Cureus
|July 19, 2023
概括
一个罕见的扩张性心肌病病例发生在一个18岁的女性身上,该病例涉及desmin (DES) 和线粒体硫素减少酶2 (TXNRD-2) 基因的突变. 这突显了细胞骨完整性与心脏病中的线粒体功能之间的潜在遗传联系.
科学领域:
- 心血管生物学 心血管生物学
- 遗传学 是一个遗传学.
- 线粒体医学 线粒体医学
背景情况:
- 德斯敏 (DES) 对于心肌细胞结构和细胞骨组织在条纹肌肉中至关重要.
- 线粒体硫素还原酶2 (TXNRD-2) 在清除线粒体氧基中起着至关重要的作用.
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