Arrhythmogenic right ventricular cardiomyopathy/dysplasia
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Key result
Arrhythmogenic right ventricular cardiomyopathy/dysplasia is a genetically determined heart muscle disease characterized by fibro-fatty replacement of the right ventricle and life-threatening arrhythmias.
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Implication
Supports genetic evaluation and imaging for suspected ARVC/D; leaves open prospective validation of screening strategies.
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Population
Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D)
This review provides a comprehensive overview of the clinical presentation, pathology, genetics, and diagnostic criteria for arrhythmogenic right ventricular cardiomyopathy/dysplasia.
Cite This Study
Thiene et al. (2007) conducted a review in Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D). Arrhythmogenic right ventricular cardiomyopathy/dysplasia is a genetically determined heart muscle disease characterized by fibro-fatty replacement of the right ventricle and life-threatening arrhythmias.
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