Brugada Syndrome: More than a Monogenic Channelopathy

Brugada Syndrome: More than a Monogenic Channelopathy

Brugada syndrome (BrS) is an inherited cardiac channelopathy first diagnosed in 1992 but still considered a challenging disease in terms of diagnosis, arrhythmia risk prediction, pathophysiology and management. Despite about 20% of individuals carrying pathogenic variants in the <i>SCN5A</i...

Full description

Bibliographic Details
Main Authors: Antonella Liantonio, Matteo Bertini, Antonietta Mele, Cristina Balla, Giorgia Dinoi, Rita Selvatici, Marco Mele, Annamaria De Luca, Francesca Gualandi, Paola Imbrici
Format: Article
Language:English
Published: MDPI AG 2023-08-01
Series:Biomedicines
Subjects:
Brugada syndrome
<i>SCN5A</i>
Nav1.5
cardiac channelopathy
arrhythmia
Online Access:https://www.mdpi.com/2227-9059/11/8/2297

Internet

https://www.mdpi.com/2227-9059/11/8/2297

Similar Items