Genetic causes of sudden cardiac death in the young

Andrea Mazzanti, Riccardo Maragna, Silvia G. Priori

Research output: Contribution to journalReview articlepeer-review


Purpose of review In this article, we discuss the most recent and relevant studies published in the field of inherited arrhythmogenic disorders, focusing in particular on channelopathies (Long QT syndrome, Brugada syndrome, and catecholaminergic polymorphic ventricular tachycardia) and arrhythmogenic right ventricular cardiomyopathy (ARVC). Recent findings We discuss the updated diagnostic criteria for channelopathies released by the European Society of Cardiology, the new results on the value of programmed electrical stimulation in patients with Brugada syndrome, and the recent evidences supporting a genotype-specific therapy for Long QT syndrome type 3. Moreover, we will present further insights into the clinical course and risk stratification of patients affected by ARVC, analyzing in particular the role of antiarrhythmic drugs for the prevention of life-threatening arrhythmias. Finally, we will explore the innovative therapeutic approaches that may be available in the future for patients with inherited arrhythmogenic disorders, such as the gene therapy. Summary The review will aid physicians in their clinical work when managing patients with inherited arrhythmias and ARVC, providing the most recent information for diagnosis, risk stratification, and management.

Original languageEnglish
Pages (from-to)253-261
Number of pages9
JournalCurrent Opinion in Cardiology
Issue number3
Publication statusPublished - May 1 2017


  • arrhythmogenic right ventricular cardiomyopathy
  • Brugada syndrome
  • catecholaminergic polymorphic ventricular tachycardia
  • Long QT syndrome
  • sudden cardiac death

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine


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