Polymorphic ventricular tachycardia

Known as: Ventricular Tachycardia, Polymorphic, Polymorphic Ventricular Tachycardia by EKG Finding, Ventricular tachycardia, polymorphous 
An electrocardiographic finding of a ventricular tachycardia in which the QRS complexes have a variable morphology and often rate. (CDISC)
National Institutes of Health

Related topics

Related topics

4 relations
Cardiovascular systemClinical Data Interchange Standards Consortium TerminologyVentricular arrhythmia

Broader (1)

Tachycardia, Ventricular

Papers overview

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2013
2013
Abnormal propagation of calcium waves and ultrastructural remodeling in recessive catecholaminergic polymorphic ventricular tachycardia.
RATIONALE The recessive form of catecholaminergic polymorphic ventricular tachycardia is caused by mutations in the cardiac… (More)
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2012
2012
Calcium leak through ryanodine receptors leads to atrial fibrillation in 3 mouse models of catecholaminergic polymorphic ventricular tachycardia.
RATIONALE Atrial fibrillation (AF) is the most common cardiac arrhythmia, however the mechanism(s) causing AF remain poorly… (More)
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Highly Cited
2006
Highly Cited
2006
Clinical phenotype and functional characterization of CASQ2 mutations associated with catecholaminergic polymorphic ventricular tachycardia.
BACKGROUND Four distinct mutations in the human cardiac calsequestrin gene (CASQ2) have been linked to catecholaminergic… (More)
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2006
2006
Genotypic heterogeneity and phenotypic mimicry among unrelated patients referred for catecholaminergic polymorphic ventricular tachycardia genetic testing.
BACKGROUND Mutations in the RyR2-encoded cardiac ryanodine receptor/calcium release channel and in CASQ2-encoded calsequestrin… (More)
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Highly Cited
2005
Highly Cited
2005
Calcium channel antagonism reduces exercise-induced ventricular arrhythmias in catecholaminergic polymorphic ventricular tachycardia patients with RyR2 mutations.
UNLABELLED Calcium channel antagonism in RyR2 defects. INTRODUCTION Recently, gain-of-function mutations of cardiac ryanodine… (More)
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2004
2004
Polymorphic ventricular tachycardia and KCNJ2 mutations.
We sought to identify the electrophysiologic basis of life-threatening events associated with polymorphic ventricular tachycardia… (More)
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2002
2002
Autosomal recessive catecholamine-induced polymorphic ventricular tachycardia.
Catecholamine-induced polymorphic ventricular tachycardia (PVT) is characterized by episodes of syncope, seizures or sudden death… (More)
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Highly Cited
2001
Highly Cited
2001
A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel.
Catecholamine-induced polymorphic ventricular tachycardia (PVT) is characterized by episodes of syncope, seizures, or sudden… (More)
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Highly Cited
2001
Highly Cited
2001
Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia.
BACKGROUND Familial polymorphic ventricular tachycardia is an autosomal-dominant, inherited disease with a relatively early onset… (More)
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Highly Cited
2001
Highly Cited
2001
Autosomal recessive catecholamine- or exercise-induced polymorphic ventricular tachycardia: clinical features and assignment of the disease gene to chromosome 1p13-21.
BACKGROUND Catecholaminergic polymorphic ventricular tachycardia (PVT) is characterized by episodes of syncope, seizures, or… (More)
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