Postoperative supraventricular tachycardia and polymorphic ventricular tachycardia due to a novel SCN5A variant: a case report of a rare comorbidity that is difficult to diagnose

BACKGROUND: Loss-of-function mutations of human cardiac sodium channel gene SCN5A induce a wide range of arrhythmic disorders. Mutation carriers with co-existing conditions such as congenital heart diseases and histories of cardiac surgeries, could develop complex arrhythmic events that are difficul...

Descripción completa

Detalles Bibliográficos
Autores principales: Kato, Koichi, Ozawa, Tomoya, Ohno, Seiko, Nakagawa, Yoshihisa, Horie, Minoru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7333335/
https://www.ncbi.nlm.nih.gov/pubmed/32615940
http://dx.doi.org/10.1186/s12872-020-01601-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7333335/
https://www.ncbi.nlm.nih.gov/pubmed/32615940
http://dx.doi.org/10.1186/s12872-020-01601-2

Ejemplares similares