Clinical Implications and Gender Differences of KCNQ1 p.Gly168Arg Pathogenic Variant in Long QT Syndrome

Clinical Implications and Gender Differences of KCNQ1 p.Gly168Arg Pathogenic Variant in Long QT Syndrome

Background: Long QT syndrome (LQTS) is an inheritable arrhythmogenic disorder associated with life-threatening arrhythmic events (LAEs). In general, patients with LQTS2 (<i>KCNH2</i>) and LQTS3 (<i>SCN5A</i>) are considered to be a greater risk of LAEs than LQTS1 (<i>KC...

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Bibliographic Details
Main Authors: Rebeca Lorca, Alejandro Junco-Vicente, Maria Martin-Fernandez, Isaac Pascual, Andrea Aparicio, Noemi Barja, Elias Cuesta-LLavona, Luis Roces, Pablo Avanzas, Cesar Moris, Eliecer Coto, José Julían Rodríguez Reguero, Juan Gómez
Format: Article
Language:English
Published: MDPI AG 2020-11-01
Series:Journal of Clinical Medicine
Subjects:
long QT syndrome
inheritable arrhythmogenic disorder
genetic testing
Online Access:https://www.mdpi.com/2077-0383/9/12/3846

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https://www.mdpi.com/2077-0383/9/12/3846

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