Related Experiment Video
Updated: Sep 27, 2026

Dual-Dye Optical Mapping of Hearts from RyR2R2474S Knock-In Mice of Catecholaminergic Polymorphic Ventricular Tachycardia
Published on: December 22, 2023
Arrhythmogenic right ventricular cardiomyopathy: three cases
Kun-Tai Lee1, Wen-Ter Lai, Hsueh-Wei Yen
1Section of Cardiology, Department of Internal Medicine, Medical University Hospital, Kaohsiung, Taiwan. kuntai.lee@msa.hinet.net
Abstract:
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a rare disease characterized by replacement of myocardium with fibrofatty tissue. It mainly involves the right ventricle (RV) and causes abnormal RV performance. ARVC is the most common cause of sudden cardiac death in young Italian athletes because it induces malignant ventricular tachyarrhythmias. Clinical manifestations of ARVC may be different between Chinese and Western patients. In this paper, we share our experience of the clinical manifestations of ARVC and review previous reports of ARVC.
Related Concept Videos
Cardiomyopathy I: Introduction and Classification
Cardiomyopathy III: Hypertrophic Cardiomyopathy
ECG Interpretation of Arrhythmias II: Atrial, Junctional and Ventricular Arrhythmias
Cardiomyopathy IV: Restrictive Cardiomyopathy
Dysrhythmias III: Characteristics of Dysrhythmias
Cardiomyopathy II: Dilated Cardiomyopathy

