Hereditary Cardiovascular Testing

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, and familial hypercholesterolemia. 
 

Ambry's inherited arrhythmia and cardiomyopathy panels feature an intuitive, tiered approach for hypertrophic cardiomyopathy, long QT syndrome, and Brugada syndrome. 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 complications.

 

Hereditary Cardiovascular Panels
Test Code Test Name Description TAT
8935 HCMFirst First-tier test of 2 most common genes for hypertrophic cardiomyopathy (HCM) 3-4 weeks
8936 HCMNext 25 genes for hypertrophic cardiomyopathy (HCM) 6-8 weeks
8883 HCMNext Reflex HCMFirst with reflex to HCMNext 6-8 weeks
8884 DCMNext 32 genes for dilated cardiomyopathy (DCM) 6-8 weeks
8886 CMNext 50 genes for inherited cardiomyopathy 6-8 weeks
8887 CMNext + TTN 51 genes for inherited cardiomyopathy 8-10 weeks
8888 RhythmFirst First-tier test of 3 genes for long QT syndrome, Brugada syndrome, short QT syndrome 3-4 weeks
8900 RhythmNext 34 genes for long QT syndrome, Brugada syndrome, other inherited arrhythmias 6-8 weeks
8901 RhythmNext Reflex RhythmFirst with reflex to RhythmNext 6-8 weeks
8902 CPVTNext 6 genes for catecholaminergic polymorphic ventricular tachycardia (CPVT) 4-6 weeks
8904 ARVDNext 8 genes for arrhythmogenic right ventricular dysplasia (ARVD) 4-6 weeks
8906 LVNCNext 4 genes for left-ventricular non-compaction (LVNC) 4-6 weeks
8910 CardioNext 83 genes for inherited cardiomyopathies and arrhythmias 8-10 weeks
8911 CardioNext + TTN 84 genes for inherited cardiomyopathies and arrhythmias 10-12 weeks
8789 TAADNext 20 genes for Marfan, thoracic aortic aneurysms and dissections (TAAD), related disorders 6-10 weeks

 

You can view a complete listing of Ambry's testing options organized by disease here, and organized by gene here.