Key result
A review of arrhythmogenic right ventricular dysplasia/cardiomyopathy highlights the pathologic and genetic basis, diagnostic features, and therapeutic challenges of the disease.
Population
Patients with Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C)
Design
Review
Authors
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ARVD/C remains diagnostically and therapeutically challenging; review extends synthesis of evidence but leaves open definitive guidelines.
This review summarizes the current understanding of the pathologic and genetic basis, diagnostic features, and therapeutic challenges of ARVD/C.
Masry et al. (2008) conducted a review in Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C). A review of arrhythmogenic right ventricular dysplasia/cardiomyopathy highlights the pathologic and genetic basis, diagnostic features, and therapeutic challenges of the disease.
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