Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2967829 | Journal of Electrocardiology | 2008 | 4 Pages |
Abstract
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.
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Authors
Okan Erdogan, Alper Aksoy, Nilda Turgut, Elcim Durusoy, Murat Samsa, Armagan Altun,