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Arrhythmogenic Ventricular Cardiomyopathy: Challenges With Complex Genetics and Variable Phenotypes
Aranyak S Rawal1, Tara VanCleave2, Neeraja Yedlapati3
1Department of Internal Medicine and Pediatrics, University of Tennessee Health Science Center, Memphis, Tennessee, USA.
Abstract:
After a 20-year-old woman suddenly died, autopsy showed characteristic findings of biventricular arrhythmogenic cardiomyopathy. Screening of her family members revealed the same desmoplakin gene mutation and imaging abnormalities predominantly involving the left ventricle. We describe the variable phenotypic expression in a family that shares a common gene variant. (Level of Difficulty: Advanced.).
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