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Clinical and molecular genetic risk determinants in adult long QT syndrome type 1 and 2 patients

Abstract Background Long QT syndrome (LQTS) is an inherited cardiac disorder predisposing to sudden cardiac death (SCD). We studied factors affecting the clinical course of genetically confirmed patients, in particular those not receiving β-blocker treatment. In addition, an attempt was made to asso...

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Principais autores: Mikael Koponen, Aki S. Havulinna, Annukka Marjamaa, Annukka M. Tuiskula, Veikko Salomaa, Päivi J. Laitinen-Forsblom, Kirsi Piippo, Lauri Toivonen, Kimmo Kontula, Matti Viitasalo, Heikki Swan
Formato: Artigo
Idioma:Inglês
Publicado em: BMC 2018-04-01
coleção:BMC Medical Genetics
Assuntos:
Long QT syndrome
Cardiac arrhythmia
Risk stratification
β-blocker
Implantable cardioverter-defibrillator
Acesso em linha:http://link.springer.com/article/10.1186/s12881-018-0574-0
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