| Literature DB >> 18353348 |
Okan Erdogan1, Alper Aksoy, Nilda Turgut, Elcim Durusoy, Murat Samsa, Armagan Altun.
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.Entities:
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Year: 2008 PMID: 18353348 DOI: 10.1016/j.jelectrocard.2008.02.023
Source DB: PubMed Journal: J Electrocardiol ISSN: 0022-0736 Impact factor: 1.438