Article
Multiple clinical profiles of families with the short QT syndrome.
Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology - 1 Jun 2018
Akdis D, Saguner A M, Medeiros-Domingo A, Schaller A, Balmer C, Steffel J, Brunckhorst C, Duru F
Abstract excerpt
Aims: Short QT syndrome (SQTS) is a rare cardiac channelopathy characterized by a shortened corrected QT (QTc)-interval that can lead to ventricular arrhythmias and sudden cardiac death. The aim of this study was to investigate the clinical phenotypes and long-term outcomes of three families harbouring genetic mutations associated with the SQTS. Methods and results: Clinical data included medical history,...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.