We are committed to providing our referring physicians with tools and resources that will enable them to make informed decisions on disease management and help stratify the risk in affected families.
We are committed to providing our referring physicians with tools and resources that will enable them to make informed decisions on disease management and help stratify the risk in affected families.
Arrhythmogenic cardiomyopathy (AC) is characterized by fibrofatty infiltration of the right ventricle. ARVC is a genetically determined heart muscle disease that extends ...
Brugada Syndrome (BrS) is an arrhythmogenic disease characterized by ST-segment elevation on ECG, incomplete right bundle-branch block, and increased risk of sudden card...
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an inherited, highly lethal arrhythmogenic cardiac disorder characterized by ventricular tachycardia in th...
Fabry disease is a lysomal storage disorder resulting from deficient or absent activity of the lysosomal enzyme, α- galactosidase A, and the resultant accumulation of gl...
Transthyretin amyloidosis, the most common form of familial amyloidosis, is a systemic disorder characterized by the extracellular deposition of amyloid fibrils causing o...
Hypertrophic cardiomyopathy (HCM), the most common of the genetic cardiovascular diseases, is characterized by heterogeneous clinical expression, unique pathophysiology a...
