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JACC Case Rep ; 3(15): 1667-1673, 2021 Nov 03.
Artigo em Inglês | MEDLINE | ID: mdl-34766015

RESUMO

Patients with familial arrhythmogenic cardiomyopathy typically present with ventricular arrhythmias or progressive heart failure. This paper characterizes a rare presentation of an underlying genetic cardiomyopathy with clinical manifestations mimicking an acute myocardial infarction in 2 siblings, each with the same mutation in the desmoplakin (DSP) gene. (Level of Difficulty: Advanced.).

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