Sex differences in long QT syndrome

Long QT Syndrome (LQTS) is a rare, inherited channelopathy characterized by cardiac repolarization dysfunction, leading to a prolonged rate-corrected QT interval in patients who are at risk for malignant ventricular tachyarrhythmias, syncope, and even sudden cardiac death. A complex genetic origin,...

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Detalles Bibliográficos
Autores principales: Díez-Escuté, Nuria, Arbelo, Elena, Martínez-Barrios, Estefanía, Cerralbo, Patricia, Cesar, Sergi, Cruzalegui, José, Chipa, Freddy, Fiol, Victoria, Zschaeck, Irene, Hernández, Clara, Campuzano, Oscar, Sarquella-Brugada, Georgia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Cardiovascular Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10110834/
https://www.ncbi.nlm.nih.gov/pubmed/37082456
http://dx.doi.org/10.3389/fcvm.2023.1164028

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10110834/
https://www.ncbi.nlm.nih.gov/pubmed/37082456
http://dx.doi.org/10.3389/fcvm.2023.1164028

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