肥厚性心肌病
MYH7
医学
心脏病学
内科学
心力衰竭
射血分数
危险分层
遗传学
磷酸化
生物
肌球蛋白轻链激酶
作者
Susumu Naito,Shuichiro Higo,Satoshi Kameda,Shou Ogawa,Tomoka Tabata,Yasuhiro Akazawa,Daisuké Nakamura,Kei Nakamoto,Fusako Sera,Yuki Kuramoto,Yoshihiro Asano,Shungo Hikoso,Shigeru Miyagawa,Yasushi Sakata
出处
期刊:Internal Medicine
[Japanese Society of Internal Medicine]
日期:2023-03-21
卷期号:62 (21): 3167-3173
被引量:4
标识
DOI:10.2169/internalmedicine.1497-22
摘要
The MYH7 R453 variant has been identified in inherited hypertrophic cardiomyopathy (HCM) and is associated with sudden death and a poor prognosis. The detailed clinical course of HCM with the MYH7 R453 variant, from a preserved to a reduced left ventricular ejection fraction, has not been reported. We identified the MYH7 R453C and R453H variants in three patients who progressively developed advanced heart failure requiring circulatory support and summarized the clinical course and echocardiographic parameters of these patients over the years. Because of the rapid disease progression, we consider genetic screening for patients with HCM imperative for future prognosis stratification.
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