Clinical Features and Outcomes of Pediatric MYH7-Related Dilated Cardiomyopathy.

doi:10.1161/JAHA.124.036208

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Article

Clinical Features and Outcomes of Pediatric MYH7-Related Dilated Cardiomyopathy.

Journal of the American Heart Association - 5 Nov 2024

de Frutos Fernando, Ochoa Juan Pablo, Webster Gregory, Jansen Mark, Remior Paloma, Rasmussen Torsten B, Sabater-Molina Maria, Barriales-Villa Roberto, Girolami Francesca, Cesar Sergi, Fuentes-Cañamero M Eugenia, Alvarez García-Rovés Reyes, Wahbi Karim, Limeres Javier, Kubanek Milos, Slieker Martijn G, Sarquella-Brugada Georgia, Abrams Dominic J, Dooijes Dennis, Domínguez Fernando, Garcia-Pavia Pablo

Abstract excerpt

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 MYH7-related DCM. METHODS AND RESULTS: We evaluated clinical records from 44 patients (24 men; median age at...

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Identifiers

PMID: 39494569
DOI: 10.1161/JAHA.124.036208

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