Brugada Phenocopy Induced by Hypovolemic Hyponatremia

Brugada syndrome (BrS) is a hereditary channelopathy caused by an autosomal dominant mutation in the cardiac sodium channel gene SCN5A alpha subunit. In individuals without structural heart disease, the risk of sudden cardiac death (SCD) increases in this channelopathy with ST-segment elevation in V...

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Detalles Bibliográficos
Autores principales: Yılmaz, Emre, Özdemir, Fatih
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Internal Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10589819/
https://www.ncbi.nlm.nih.gov/pubmed/37868457
http://dx.doi.org/10.7759/cureus.45667

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10589819/
https://www.ncbi.nlm.nih.gov/pubmed/37868457
http://dx.doi.org/10.7759/cureus.45667

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