Complex atrial arrhythmias as first manifestation of catecholaminergic polymorphic ventricular tachycardia: an unusual course in a patient with a new mutation in ryanodine receptor type 2 gene.

Abstract:

:Catecholaminergic polymorphic ventricular tachycardia is a rare life-threatening arrhythmogenic disorder. An association with paroxysmal atrial fibrillation and other atrial arrhythmias has been described, but in all published cases the initial manifestation of the disease was ventricular arrhythmia. This is the first report about a patient who presented with complex atrial tachycardia and sinus node dysfunction about 1 year before the typical ventricular arrhythmias were observed, leading to the diagnosis of catecholaminergic polymorphic ventricular tachycardia. In this girl, a mutation of the ryanodine receptor type 2 gene, which has not been described so far, was discovered.

journal_name

Cardiol Young

journal_title

Cardiology in the young

authors

Lawrenz W,Krogmann ON,Wieczorek M

doi

10.1017/S1047951113001091

subject

Has Abstract

pub_date

2014-08-01 00:00:00

pages

741-4

issue

4

eissn

1047-9511

issn

1467-1107

pii

S1047951113001091

journal_volume

24

pub_type

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