Genetic Arrhythmia

The identification for the  genetic substrate underlying the inherited arrhythmia syndromes which has provided remarkable insight  the molecular basis of the cardiac electrophysiology, including the role of the various ion channels and mechanisms of arrhythmias. The availability of genetic diagnostic test has added an important diagnostic tool, providing new opportunities for patient responsibility such as early (presymptomatic) identification and treatment of individuals at risk of developing fatal arrhythmias. Brugada syndrome is the genetic disease that is characterized by an abnormal electrocardiogram (ECG) findings and an increased risk of sudden cardiac deaths where long QT syndrome (LQTS) is a disorder of the heart's electrical activity. It  cause sudden, uncontrollable, dangerous arrhythmia in response to exercise or stress and short QT syndrome is the condition that can cause  disruption of the heart's normal rhythm (arrhythmia).

Related Conference: Eighth Global Cardiologists Annual Meeting during July 18-20, 2016 Berlin, Germany; 11th  International Cardiac Conference September 14 -15, 2016 Philadelphia, USA; 8th International Conference on  Clinical and Experimental Cardiology November 14-16, 2016 San Francisco, USA; 7th World Cardio-thoracic Meeting December 5 - 6, 2016, Philadelphia, USA; 12th World Cardiology Congress during October 10–12, 2016 Manchester, UK; Symposium in Structural Heart disease Interventions  January 21-22, 2016 in Celebration, USA; International Stroke Conference February 17-19, 2016 Los Angeles, USA; Cardiology Issues in Younger Adults during September 15-24, 2016 Rome, Italy; World Conference in Cardiac Electrophysiology and Cardiac Techniques June 8-11, 2016 Nice, France; 65th Annual Scientific Session and Expo on Cardiology in American College April 02-04,2016 Chicago, USA.

In genetic arrhythmia various syndrome are their like Long QT Syndrome (LQTS) is a rare inherited or acquired heart condition in which delayed repolarization of the heart following a heartbeat increases the risk of episodes of torsades de pointes ( a form of irregular heartbeat that originates from the ventricles), then in  Short QT Syndrome  genetic disease of the electrical system of the heart and  in Brugada Syndrome (BrS)  genetic disease that is characterised by abnormal electrocardiogram (ECG) findings and an increased risk of sudden cardiac death.

  • Long QT syndrome
  • Short QT syndrome
  • Brugada syndrome

Related Conference of Genetic Arrhythmia

Genetic Arrhythmia Conference Speakers