Langt QT-syndrom--gener, mekanismer og risici. Indikation for genetisk familieudredning?

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Inherited long QT syndrome (LQTS) is a cardiac disease characterised by episodes of ventricular tachyarrhythmia, presenting as syncope or sudden death. Untreated, the annual mortality rate is 1-2%. Sudden death has been reported as the first manifestation of the disease in some cases. Therefore, early (pre-symptomatic) diagnosis and management may save lives. However, clinically false negative relatives are also at risk of sudden death. On this basis we conclude assessment of relatives should be extended with genetic testing.
Udgivelsesdato: 2006-Jun-26
Translated title of the contributionLong QT syndrome--genes, mechanisms and risks. Indication for genetic family screening?
Original languageDanish
JournalUgeskrift for læger
Volume168
Issue number26-32
Pages (from-to)2537-42
Number of pages5
ISSN0041-5782
Publication statusPublished - 2006

Bibliographical note

Keywords: Death, Sudden, Cardiac; Genetic Predisposition to Disease; Genetic Testing; Humans; Ion Channels; Long QT Syndrome; Risk Factors; Syncope

ID: 21258917