Structural Heart Alterations in Brugada Syndrome: Is it Really a Channelopathy? A Systematic Review

Brugada syndrome (BrS) is classified as an inherited cardiac channelopathy attributed to dysfunctional ion channels and/or associated proteins in cardiomyocytes rather than to structural heart alterations. However, hearts of some BrS patients exhibit slight histologic abnormalities, suggesting that...

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Detalles Bibliográficos
Autores principales: Oliva, Antonio, Grassi, Simone, Pinchi, Vilma, Cazzato, Francesca, Coll, Mónica, Alcalde, Mireia, Vallverdú-Prats, Marta, Perez-Serra, Alexandra, Martínez-Barrios, Estefanía, Cesar, Sergi, Iglesias, Anna, Cruzalegui, José, Hernández, Clara, Fiol, Victoria, Arbelo, Elena, Díez-Escuté, Nuria, Arena, Vincenzo, Brugada, Josep, Sarquella-Brugada, Georgia, Brugada, Ramon, Campuzano, Oscar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Systematic Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9368908/
https://www.ncbi.nlm.nih.gov/pubmed/35956023
http://dx.doi.org/10.3390/jcm11154406

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9368908/
https://www.ncbi.nlm.nih.gov/pubmed/35956023
http://dx.doi.org/10.3390/jcm11154406

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