Clinical phenotype and diagnosis of arrhythmogenic right ventricular cardiomyopathy in pediatric patients carrying desmosomal gene mutations

BACKGROUND: Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited heart muscle disease carrying a risk of sudden death. Information about the clinical features during childhood and the age at disease onset is scanty. OBJECTIVE: The aim of the study was to describe the ARVC phenotype...

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Detalles Bibliográficos
Autores principales: Bauce, Barbara, Rampazzo, Alessandra, Basso, Cristina, Mazzotti, Elisa, Rigato, Ilaria, Steriotis, Alexandros, Beffagna, Giorgia, Lorenzon, Alessandra, De Bortoli, Marzia, Pilichou, Kalliopi, Marra, Martina Perazzolo, Corbetti, Francesco, Daliento, Luciano, Iliceto, Sabino, Corrado, Domenico, Thiene, Gaetano, Nava, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2011
Materias:
Clinical
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3205183/
https://www.ncbi.nlm.nih.gov/pubmed/21723241
http://dx.doi.org/10.1016/j.hrthm.2011.06.026

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3205183/
https://www.ncbi.nlm.nih.gov/pubmed/21723241
http://dx.doi.org/10.1016/j.hrthm.2011.06.026

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