Syncope in Hereditary Arrhythmogenic Syndromes - 29/06/15
Doi : 10.1016/j.ccl.2015.04.011
Arnon Adler, MD, Sami Viskin, MD ⁎ 
Sackler School of Medicine, Tel Aviv Medical Center, Tel Aviv University, Israel
∗Corresponding author. Department of Cardiology, Tel Aviv Medical Center, Weizman 6, Tel Aviv 64239, Israel.
Résumé |
Since the discovery of the first mutation causing long QT syndrome (LQTS) in 1995, the field of hereditary arrhythmogenic syndromes has expanded greatly. Today, these syndromes include LQTS, Brugada syndrome, catecholaminergic polymorphic ventricular tachycardia, and short QT syndrome. There is also evidence suggesting that the newly described malignant early repolarization syndrome also has a genetic cause.
Le texte complet de cet article est disponible en PDF.Keywords : Arrhythmogenic syndrome, Syncope, Genotype, Follow-up
Plan
| This article originally appeared in Cardiac Electrophysiology Clinics, Volume 5, Issue 4, December 2013. |
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| Conflicts of Interest: None. |
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| Sources of Specific Funding: None. |
© 2015
Elsevier Inc. Tous droits réservés.
Vol 33 - N° 3
P. 433-440 - août 2015 Retour au numéro
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