Cardiovascular Genetics

Cardiovascular genetics is the study of family genetics to offer a complete evaluation, diagnosis and disease management remedy for people who are at danger or risk for or have inherited a cardiovascular disorder. Heritable factors inherit a number of cardiovascular diseases like diseases of the heart’s muscle, vasculature and electrical system. These inherited heart conditions, referred as cardiovascular genetic disorders, may overlooked and undiagnosed for years before being recognized or causing symptoms. In Cardiovascular Medicine Conference, Cardiovascular genetics is one of our special track which carries many unanswered topics related to research in cardiovascular genetics, genomics, systems biology, metabolomics, novel biomarkers  and proteomics that will enhance the understanding of the pathophysiological basis of cardiovascular disorders which contribute to the prevention, diagnosis, screening, risk stratification, and management of cardiovascular disease. Special sections under Cardiovascular Genetics are genetic linkage and clinical proteomics, candidate genes, perturbations, regulation of gene expression, gene therapy, pharmacogenomics, epigenetics, metabolomics, and systems biology approach to diagnosis and management of cardiovascular disorders.

  • Dilated cardiomyopathy (DCM)
  • Hypoplastic left heart syndrome (HLHS)
  • Spontaneous coronary artery dissection (SCAD)
  • Genetic epidemiology and translational cardiovascular genomics
  • Hypercholesterolemia and hypertrophic cardiomyopathy
  • Energy Medicine

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