Identifying genomic variant associated with long QT syndrome type 2 in an ecuadorian mestizo individual: a case report

IntroductionLong QT syndrome (LQTS) is an autosomal dominant inherited cardiac condition characterized by a QT interval prolongation and risk of sudden death. There are 17 subtypes of this syndrome associated with genetic variants in 11 genes. The second most common is type 2, caused by a mutation i...

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Bibliographic Details

Published in:	Frontiers in Genetics
Main Authors:	Rafael Tamayo-Trujillo, Rita Ibarra-Castillo, José Luis Laso-Bayas, Patricia Guevara-Ramirez, Santiago Cadena-Ullauri, Elius Paz-Cruz, Viviana A. Ruiz-Pozo, Nieves Doménech, Adriana Alexandra Ibarra-Rodríguez, Ana Karina Zambrano
Format:	Article
Language:	English
Published:	Frontiers Media S.A. 2024-06-01
Subjects:	implantable defibrillator long QT syndrome NGS kcnh2 case report
Online Access:	https://www.frontiersin.org/articles/10.3389/fgene.2024.1395012/full