Cardiomyopathy is defined as disease of the heart muscle and has many different presentations. This test provides a comprehensive analysis of the genes associated with inherited cardiomyopathy conditions. Given the clinical overlap between different cardiomyopathy conditions, comprehensive testing enables a more efficient evaluation of multiple conditions based on a single indication. Individuals with clinical symptoms of an inherited cardiomyopathy may benefit from diagnostic genetic testing to establish or confirm diagnosis, clarify risks, or inform management. Asymptomatic individuals within a family with a known pathogenic variant may also benefit by avoiding activities and medications that can trigger symptoms.
We analyze additionally More Than 60 genes related Hypertrophic cardiomyopathy (HCM),Dilated cardiomyopathy (DCM), Left ventricular non-compaction (LVNC), Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVC) and Noonan syndrome (NS).
Report Delivery
+5 Work Days
Sample Type
Depends on the test tipe
