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Genetic testing for long QT syndrome and the category of cardiac ion channelopathies
Author(s) -
Stephen M. Modell,
David J. Bradley,
Michael H. Lehmann
Publication year - 2012
Publication title -
plos currents
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.282
H-Index - 49
ISSN - 2157-3999
DOI - 10.1371/4f9995f69e6c7
Subject(s) - catecholaminergic polymorphic ventricular tachycardia , long qt syndrome , medicine , brugada syndrome , sudden cardiac death , genetic testing , short qt syndrome , sudden death , cardiology , channelopathy , implantable cardioverter defibrillator , ventricular tachycardia , qt interval , ryanodine receptor 2 , ryanodine receptor , calcium
Cardiac ion channel mutational analysis is a category of genetic testing used in clinical practice for determining the status of long QT syndrome, short QT syndrome, catecholaminergic polymorphic ventricular tachycardia, and Brugada syndrome genes in blood, saliva, or tissue from patients and family members at risk for cardiac events such as syncope and sudden death. Such testing is most informative following careful phenotypic characterization. Individuals with ion channelopathies may benefit from prevention (avoidance of triggers and predisposing drugs) and treatment (e.g., beta blocker therapy, implantable cardioverter-defibrillator (ICD) placement) modalities.

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