Journal of Electrocardiology, cilt.41, sa.4, ss.325-328, 2008 (SCI-Expanded, Scopus)
Andersen-Tawil syndrome (ATS) is a rare, heterogeneous, autosomal dominant, or sporadic disorder characterized by the clinical triad of periodic paralysis, dysmorphic features, and ventricular arrhythmias such as bidirectional ventricular tachycardia (BVT). We present a case of an elderly patient with ATS whose symptomatic ventricular arrhythmias including BVT were effectively suppressed by oral verapamil therapy. © 2008 Elsevier Inc. All rights reserved.