[Molecular genetics of cardiac arrhythmias] - Inserm - Institut national de la santé et de la recherche médicale Access content directly
Journal Articles La Revue de Médecine Interne Year : 2006

[Molecular genetics of cardiac arrhythmias]


INTRODUCTION: Recent progress in molecular biology led to the identification of the genes involved in various cardiac arrhythmias causing syncope and sudden death in young people. EXEGESIS: This article briefly describes the clinical features and the genes associated with the congenital long QT syndrome, the short QT syndrome, Brugada's syndrome, catecholaminergic polymorphic ventricular tachycardias and arrhythmogenic right ventricular dysplasia. CONCLUSION: Identification of genetic variations that cause cardiac tachyarrhythmias can help to identify at risk-patients and to propose clinical follow-up and preventive therapy. Further studies are needed to discover other cardiac genetic disorders and to understand cellular mechanisms involved in these diseases.
Embargoed file
Embargoed file
Visibility date is undetermined

Dates and versions

inserm-00383903 , version 1 (09-07-2009)



Claire Thomas, Pascale Guicheney, Joël Lunardi. [Molecular genetics of cardiac arrhythmias]. La Revue de Médecine Interne, 2006, 27 (3), pp.236-9. ⟨10.1016/j.revmed.2005.10.012⟩. ⟨inserm-00383903⟩
84 View
1 Download



Gmail Mastodon Facebook X LinkedIn More