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Clinical Features and Outcomes of Pediatric MYH7‐Related Dilated Cardiomyopathy

Background Although genetic variants in MYH7 are the most frequent cause of pediatric genetic dilated cardiomyopathy (DCM), there are no studies available describing this entity. We sought to describe clinical features, analyze variant location, and explore predictors of bad prognosis in pediatric M...

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Asıl Yazarlar: Fernando de Frutos, Juan Pablo Ochoa, Gregory Webster, Mark Jansen, Paloma Remior, Torsten B. Rasmussen, Maria Sabater‐Molina, Roberto Barriales‐Villa, Francesca Girolami, Sergi Cesar, M. Eugenia Fuentes‐Cañamero, Reyes Alvarez García‐Rovés, Karim Wahbi, Javier Limeres, Milos Kubanek, Martijn G. Slieker, Georgia Sarquella‐Brugada, Dominic J. Abrams, Dennis Dooijes, Fernando Domínguez, Pablo Garcia‐Pavia
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Wiley 2024-11-01
Seri Bilgileri:Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Konular:
dilated cardiomyopathy
genetics
MYH7
pediatric
Online Erişim:https://www.ahajournals.org/doi/10.1161/JAHA.124.036208
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