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
Autores principales: Rawal, Aranyak S., VanCleave, Tara, Yedlapati, Neeraja, Saffitz, Jeffery E., Craigen, William James, Jefferies, John L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Mini-Focus Issue: Heart Failure
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8311029/
https://www.ncbi.nlm.nih.gov/pubmed/34317553
http://dx.doi.org/10.1016/j.jaccas.2020.12.012

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8311029/
https://www.ncbi.nlm.nih.gov/pubmed/34317553
http://dx.doi.org/10.1016/j.jaccas.2020.12.012

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