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Updated: Jun 10, 2026

Dual-Dye Optical Mapping of Hearts from RyR2R2474S Knock-In Mice of Catecholaminergic Polymorphic Ventricular Tachycardia
Published on: December 22, 2023
[Arrhythmogenic cardiomyopathy with predominant left ventricular involvement]
Farid Aliyev1, Cengizhan Türkoğlu, Cengiz Celiker
1Istanbul Universitesi Kardiyoloji Enstitüsü Kardiyoloji Anabilim Dali, Istanbul, Turkey. drfaridaliyev@yahoo.com.tr
Abstract:
Arrhythmogenic right ventricular cardiomyopathy is a relatively well-defined clinical entity. This disease is characterized with right ventricular involvement and is an important cause of sudden cardiac death in young patients. However, arrhythmogenic cardiomyopathy with left-dominant involvement has recently been better described in the literature. This new presentation may be confused with other diseases such as idiopathic dilated cardiomyopathy. This review outlines left-dominant arrhythmogenic cardiomyopathy in the light of the most recent information.
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