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

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

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
Bidragets oversatte titelLong QT syndrome--genes, mechanisms and risks. Indication for genetic family screening?
OriginalsprogDansk
TidsskriftUgeskrift for læger
Vol/bind168
Udgave nummer26-32
Sider (fra-til)2537-42
Antal sider5
ISSN0041-5782
StatusUdgivet - 2006

ID: 21258917