Case report: State-of-the-art risk-modifying treatment of sudden cardiac death in an asymptomatic patient with a mutation in the SCN5A gene and a review of the literature

Brugada syndrome is a rare hereditary disorder characterized by distinct ECG findings, complex genetics, and a high risk of sudden cardiac death. Recognition of the syndrome is crucial as it represents a paradigm of sudden death tragedy in individuals at the peak of their lives. Notably, Brugada syn...

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Detalles Bibliográficos
Autores principales: Brlek, Petar, Pavelić, Eduard Stjepan, Mešić, Jana, Vrdoljak, Kristijan, Skelin, Andrea, Manola, Šime, Pavlović, Nikola, Ćatić, Jasmina, Matijević, Gordana, Brugada, Josep, Primorac, Dragan
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/PMC10512029/
https://www.ncbi.nlm.nih.gov/pubmed/37745129
http://dx.doi.org/10.3389/fcvm.2023.1193878

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10512029/
https://www.ncbi.nlm.nih.gov/pubmed/37745129
http://dx.doi.org/10.3389/fcvm.2023.1193878

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