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

February 19-21, 2018

23rd European Heart Disease and Heart Failure Congress

Paris, France
April 19-20, 2018

3rd World Heart Congress

Amsterdam, Netherlands
May 14-16, 2018

2nd World Heart Congress

Tokyo, Japan
June 11-13, 2018

24th Annual Cardiologists Conference

Barcelona, Spain
July 12-13, 2018

Global Cardiology Summit

Bangkok, Thailand
August 09-10, 2018

26th Annual Cardiology and Cardiovascular  Nursing Congress

Manila, Philippines
September 10-11, 2018

4th International Conference on Hypertension & Healthcare

Zurich, Switzerland
September 11-12, 2018

World Cardiology and Cardiologist Meeting

Stockholm, Sweden
September 14-15, 2018

4th Global Summit on Heart Diseases

Singapore
17-18 September,2018

24th World Cardiology Conference

Hong Kong
September 17-18,2018

25th Annual Cardiologists Conference

Tin Shui Wai,Hong Kong
September 21-22, 2018

27th International Conference on Clinical & Experimental Cardiology Research

Vancouver, British Columbia, Canada
September 24-26, 2018

5th World Heart and Brain Conference

Abu Dhabi, UAE
October 22-24, 2018

27th European Cardiology Conference

Rome, Italy
October 22-24, 2018

27th European Cardiology Conference

Rome, Italy
October 25-27, 2018

World Heart Rhythm Conference

Istanbul, Turkey
November 5-6, 2018

28thWorld Congress on Cardiology and Heart Diseases

Amsterdam, Netherlands
November 19-20, 2018

29th World Cardiology Conference

Edinburgh, Scotland

Genetic Arrhythmia Conference Speakers

Recommended Sessions

Related Journals

Are you interested in