Article
Natural History of MYH7-Related Dilated Cardiomyopathy.
Journal of the American College of Cardiology - 11 Oct 2022
de Frutos Fernando, Ochoa Juan Pablo, Navarro-Peñalver Marina, Baas Annette, Bjerre Jesper Vandborg, Zorio Esther, Méndez Irene, Lorca Rebeca, Verdonschot Job A J, García-Granja Pablo Elpidio, Bilinska Zofia, Fatkin Diane, Fuentes-Cañamero M Eugenia, García-Pinilla José M, García-Álvarez María I, Girolami Francesca, Barriales-Villa Roberto, Díez-López Carles, Lopes Luis R, Wahbi Karim, García-Álvarez Ana, Rodríguez-Sánchez Ibon, Rekondo-Olaetxea Javier, Rodríguez-Palomares José F, Gallego-Delgado María, Meder Benjamin, Kubanek Milos, Hansen Frederikke G, Restrepo-Córdoba María Alejandra, Palomino-Doza Julián, Ruiz-Guerrero Luis, Sarquella-Brugada Georgia, Perez-Perez Alberto José, Bermúdez-Jiménez Francisco José, Ripoll-Vera Tomas, Rasmussen Torsten Bloch, Jansen Mark, Sabater-Molina Maria, Elliot Perry M, Garcia-Pavia Pablo
Abstract excerpt
BACKGROUND: Variants in myosin heavy chain 7 (MYH7) are responsible for disease in 1% to 5% of patients with dilated cardiomyopathy (DCM); however, the clinical characteristics and natural history of MYH7-related DCM are poorly described. OBJECTIVES: We sought to determine the phenotype and prognosis of MYH7-related DCM. We also evaluated the influence of variant location on phenotypic expression. METHODS: We...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.