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Arrhythmogenic Ventricular Cardiomyopathy: Challenges With Complex Genetics and Variable Phenotypes

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 p...

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Detalles Bibliográficos
Publicado en:JACC Case Rep
Main Authors: Rawal, Aranyak S., VanCleave, Tara, Yedlapati, Neeraja, Saffitz, Jeffery E., Craigen, William James, Jefferies, John L.
Formato: Artigo
Idioma:Inglês
Publicado: Elsevier 2021
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC8311029/
https://ncbi.nlm.nih.gov/pubmed/34317553
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jaccas.2020.12.012
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