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Ambry's inherited arrhythmia and cardiomyopathy panels feature an intuitive, tiered approach. Establishing a molecular diagnosis for inherited cardiovascular conditions can be life-saving; genetic test results can direct and improve patient management, and target surveillance for cardiovascular complication.

Ambry’s hereditary cardiovascular testing menu includes multi-gene panels and single gene testing for inherited arrhythmias, cardiomyopathies, aortic aneurysms/dissections, Marfan syndrome, Ehlers-Danlos syndromes, familial hypercholesterolemia, hereditary hemorrhagic telangiectasia, and transthyretin amyloidosis.

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