Genetic and inherited heart diseases are a group of conditions that result from abnormalities in the genetic code, affecting the structure and function of the heart. These diseases, such as familial hypercholesterolemia, hypertrophic cardiomyopathy, and arrhythmogenic right ventricular dysplasia, are passed down through families and often present early in life. Early detection through genetic screening and family history assessment can help identify individuals at risk and enable timely interventions. Personalized treatments, including medication, lifestyle changes, and in some cases, genetic therapies, are essential for managing these conditions. Understanding the genetic basis of heart disease is key to preventing the onset of symptoms, improving outcomes, and reducing the risk of sudden cardiac events.
Title : Surgical fetal stem cells implantation in heart failure patients long term results at 14 years
Federico Benetti, Benetti Foundation, Argentina
Title : Exploring new biomarkers of cardiomyopathy
Shuping Zhong, University of Southern California, United States
Title : The development of human relaxin-2 for heart failure with preserved ejection fraction, HFpEF
Thomas Bernd Dschietzig, Relaxera GmbH & Co. KG, Germany
Title : Cancer and cardiovascular diseases: Common pathogenesis mechanisms and risk factors
Mekhman N Mamedov, National Research Center for Preventive Medicine, Russian Federation
Title : Pulse field ablation for atrial fibrillation complications: What do we know yet
Narendra Kumar, HeartbeatsZ Academy, United Kingdom
Title : Lipoprotein (a): The hidden cardiovascular risk
Syed Raza, Awali Hospital, Bahrain