Erdogan, OkanAksoy, AlperTurgut, NildaDurusoy, ElcimSamsa, MuratAltun, Armagan2024-06-122024-06-1220080022-0736https://doi.org/10.1016/j.jelectrocard.2008.02.023https://hdl.handle.net/20.500.14551/18438Andersen-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. (C) 2008 Elsevier Inc. All rights reserved.en10.1016/j.jelectrocard.2008.02.023info:eu-repo/semantics/closedAccessAndersen-TawilVerapamilBidirectional VTU WaveLong QTTherapySudden DeathKcnj2 MutationsTachycardiaArticle414325328Q3WOS:0002573496000132-s2.0-4504908640118353348Q3