Multiple clinical profiles of families with the short QT syndrome
D Akdis, AM Saguner, A Medeiros-Domingo… - EP …, 2018 - academic.oup.com
Abstract 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 …
a shortened corrected QT (QTc)-interval that can lead to ventricular arrhythmias and sudden …
Dilated cardiomyopathy with short QT interval: is it a new clinical entity?
S Bohora, N Namboodiri, J Tharakan… - Pacing and clinical …, 2009 - Wiley Online Library
Short QT syndrome is a rare autosomal dominant channelopathy of structurally normal
hearts characterized by atrial fibrillation, ventricular arrhythmias, and sudden cardiac death …
hearts characterized by atrial fibrillation, ventricular arrhythmias, and sudden cardiac death …
Ventricular fibrillation in a family with short QT syndrome type 2 carrying a heterozygous KCNQ1-V141M variant
F Takechi, K Kato, T Makiyama, S Ohno… - Journal of Pediatric …, 2022 - jstage.jst.go.jp
Short QT syndrome (SQTS) is an inheritable cardiac electrical disease presenting both atrial
and ventricular arrhythmias associated with abnormally short QT intervals on …
and ventricular arrhythmias associated with abnormally short QT intervals on …
Electrocardiographic manifestations: long QT Syndrome
EM Mancuso, WJ Brady, RA Harrigan, M Pollack… - The Journal of …, 2004 - Elsevier
Long QT Syndrome is a cardiac disorder caused by an abnormal prolongation of the
ventricular repolarization phase. The primary concern in this syndrome is the propensity …
ventricular repolarization phase. The primary concern in this syndrome is the propensity …
Diagnosis and management of short QT syndrome
P Bjerregaard - Heart Rhythm, 2018 - Elsevier
Establishing a definition of short QT syndrome (SQTS), including symptomatology and QT-
interval duration, is still a work in progress. However, it is clear, that SQTS is a rare, life …
interval duration, is still a work in progress. However, it is clear, that SQTS is a rare, life …
Long and short QT syndromes: Emergency treatment and secondary prophylaxis
N Horn, N Rüb, C Wolpert - Herzschrittmachertherapie+ Elektrophysiologie, 2020 - Springer
Long QT syndrome (LQTS) is a rare inherited or acquired channelopathy associated with a
relevant mortality if left untreated. Therapy can reduce the sudden cardiac death (SCD) rate …
relevant mortality if left untreated. Therapy can reduce the sudden cardiac death (SCD) rate …
Congenital short QT syndrome. A review.
C Ginghină, R Ciudin, O Lăpuşanu… - Romanian Journal of …, 2005 - europepmc.org
Sudden cardiac death in individuals with structurally normal hearts accounts for
approximately 20% of sudden cardiac death cases. Patients in this subgroup suffer from …
approximately 20% of sudden cardiac death cases. Patients in this subgroup suffer from …
The dark side of the QT interval. The Short QT Syndrome: pathophysiology, clinical presentation and management
I Comelli, G Lippi, G Mossini, G Gonzi… - Emergency Care …, 2012 - pagepressjournals.org
A large number of studies has been carried out to investigate the pathophysiology and the
clinical implications of QT interval prolongation in the ECG over recent years (1, 2, 3, 4, 5, 6) …
clinical implications of QT interval prolongation in the ECG over recent years (1, 2, 3, 4, 5, 6) …
[HTML][HTML] A case of long QT syndrome type 2 that developed torsades de pointes two days after the initiation of oral β-blocker therapy
F Yoneda, T Makiyama, K Miyahara, Y Fukuoka… - HeartRhythm Case …, 2022 - Elsevier
Congenital long QT syndrome (LQT) is a potentially lethal hereditary arrhythmic disorder that
can cause syncope and sudden cardiac death owing to polymorphic ventricular …
can cause syncope and sudden cardiac death owing to polymorphic ventricular …