Brugada综合征
导航1.5
医学
钠通道
心肌病
心脏病学
内科学
表型
心功能曲线
植入式心律转复除颤器
基因
钠
遗传学
心力衰竭
生物
有机化学
化学
作者
Tanja Charlotte Frederiksen,Kirstine Calløe,Michelle Geryk,Henrik Kjærulf Jensen
标识
DOI:10.1016/j.hrcr.2022.01.017
摘要
Key Teaching Points•We found a novel variant in the SCN5A gene (p. Arg376Leu (R376L)) in a patient with a coexistence of Brugada syndrome and takotsubo cardiomyopathy.•Electrophysiological investigations are consistent with a loss of function in the cardiac sodium channel Nav1.5.•This case report highlights the uncertainty that follows the finding of rare genetic variants and coexisting phenotypes. •We found a novel variant in the SCN5A gene (p. Arg376Leu (R376L)) in a patient with a coexistence of Brugada syndrome and takotsubo cardiomyopathy.•Electrophysiological investigations are consistent with a loss of function in the cardiac sodium channel Nav1.5.•This case report highlights the uncertainty that follows the finding of rare genetic variants and coexisting phenotypes.
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