Publication
Title
Sudden cardiac death : what is inside our genes?
Author
Abstract
Although sudden cardiac death in youths is generally rare, it is estimated that 10% to 20% of these deaths occur in previously healthy infants, children, adolescents and young adults without any findings on autopsy and with devastating consequences on the family. The majority of these deaths are caused by inherited arrhythmia syndromes, the so-called 'channelopathies'. In the present paper, the recent advances in the clinical and genetic background of long QT syndrome, short QT syndrome, catecholaminergic polymorphic ventricular tachycardia, Brugada syndrome and the overlapping phenotypes are reviewed, and the recently established connections between these syndromes and idiopathic ventricular fibrillation and sudden infant death syndrome are discussed.
Language
English
Source (journal)
Canadian journal of cardiology. - Oakville, Ont.
Source (book)
58th Annual Meeting of the Canadian-Cardiovascular-Society, OCT 23, 2005, Montreal, CANADA
Publication
Oakville : Pulsus group inc , 2005
ISSN
0828-282X
Volume/pages
21 :12 (2005) , p. 1099-1110
ISI
000232871000018
Pubmed ID
16234896
UAntwerpen
Publication type
Subject
External links
Web of Science
Record
Identifier
Creation 21.04.2020
Last edited 18.12.2024
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