在HCM中ATTR基因变异
Anthony J Kanelidis1, Jeremy A Slivnick1, Rachel Campagna1
1University of Chicago Medicine, Chicago, Illinois, USA.
JACC. Case reports
|March 29, 2024
概括
过度缩性心肌病变 (HCM) 通常是遗传的. 然而,TTR基因变异导致心脏粉症可以模仿HCM,突出显示一个未被认可的诊断重叠.
科学领域:
- 心脏病学 心脏病学
- 遗传学 是一个遗传学.
- 分子生物学分子生物学
背景情况:
- 增高性心肌病变 (HCM) 是最常见的遗传性心脏病,影响200人中的1人到500人中的1人.
- 心脏 Amyloidosis 涉及错误折叠的 transthyretin (TTR) 蛋白在心肌中的沉积,导致心肌病变.
- 氨基粉症可以是获得的或遗传的,呈现诊断挑战.
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