Symptomatic sinus bradycardia, due to either sick sinus syndrome or vagotonia, can be familial, affecting several members of a family. We report an 18-year-old male patient with palpitations and limited exercise capacity who was noted to have severe sinus bradycardia. His resting heart rate was 40/min, with normal PR and corrected QT intervals, and sinus pauses up to 6 seconds during sleep. Exercise treadmill test and pharmacologic autonomic blockade during electrophysiologic studies abolished the bradycardia, suggestive of vagotonia rather than intrinsic sinus node dysfunction. This patient\u27s father and a female cousin had a similar clinical history but associated with syncope and severe sinus bradycardia. The mode of transmission appea...
Background-Sick sinus syndrome (SSS) is a common arrhythmia often associated with aging or organic h...
Background-Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an inherited arrhythmia s...
Introduction: We recently identified a novel mutation of SCN5A (1795insD) in a large family with fea...
Introduction: Sinus bradycardia is a common entity encountered in clinical practice. The differentia...
A symptomatic sinus bradycardia is a very common situation in cardiology for which the diagnostic an...
none9noWe report the case of a boy who was first addressed to medical attention when he was 2-years-...
A family is reported in which the diagnosis of sinuatrial disorder was present in both the original ...
Sick sinus syndrome (SSS) describes an arrhythmia phenotype attributed to dysfunction of sinus node....
WOS: 000374330000030PubMed: 25744562Patient: Male, 22 Final Diagnosis: Sinus node dysfunction Sympto...
BACKGROUND: Inherited arrhythmias were originally considered isolated electrical defects. There is g...
BACKGROUND: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an inherited arrhythmia ...
The commonly proposed mechanism of syncope in patients (pts) with sick sinus syndrome (SSS) is a lon...
Congenital long-QT syndrome (LQTS) is an inherited cardiac disorder characterized by the prolongatio...
AbstractBackgroundInherited arrhythmias were originally considered isolated electrical defects. Ther...
An asymptomatic 5-year-old girl presented with bradycardia during a routine well-child visit. Furthe...
Background-Sick sinus syndrome (SSS) is a common arrhythmia often associated with aging or organic h...
Background-Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an inherited arrhythmia s...
Introduction: We recently identified a novel mutation of SCN5A (1795insD) in a large family with fea...
Introduction: Sinus bradycardia is a common entity encountered in clinical practice. The differentia...
A symptomatic sinus bradycardia is a very common situation in cardiology for which the diagnostic an...
none9noWe report the case of a boy who was first addressed to medical attention when he was 2-years-...
A family is reported in which the diagnosis of sinuatrial disorder was present in both the original ...
Sick sinus syndrome (SSS) describes an arrhythmia phenotype attributed to dysfunction of sinus node....
WOS: 000374330000030PubMed: 25744562Patient: Male, 22 Final Diagnosis: Sinus node dysfunction Sympto...
BACKGROUND: Inherited arrhythmias were originally considered isolated electrical defects. There is g...
BACKGROUND: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an inherited arrhythmia ...
The commonly proposed mechanism of syncope in patients (pts) with sick sinus syndrome (SSS) is a lon...
Congenital long-QT syndrome (LQTS) is an inherited cardiac disorder characterized by the prolongatio...
AbstractBackgroundInherited arrhythmias were originally considered isolated electrical defects. Ther...
An asymptomatic 5-year-old girl presented with bradycardia during a routine well-child visit. Furthe...
Background-Sick sinus syndrome (SSS) is a common arrhythmia often associated with aging or organic h...
Background-Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an inherited arrhythmia s...
Introduction: We recently identified a novel mutation of SCN5A (1795insD) in a large family with fea...