Order DCM/Arrhythmogenic Cardiomyopathy Panel (53 Genes) Test
Dilated cardiomyopathy (DCM) is characterized by ventricular chamber enlargement and systolic dysfunction with normal left ventricular wall thickness. Arrhythmogenic cardiomyopathies (AC) encompass a spectrum of diseases, the classic form of which is arrhythmogenic right ventricular cardiomyopathy (ARVC), though recognition of phenotypic variability recently prompted adoption of a broader term. Read more details about this test.
All samples must be accompanied with a completed requisition form. Please make sure any identifiers used on the specimen are provided on the paperwork. Consent page should be signed by a health care provider. Any incomplete or missing paperwork may delay the start of testing.
ABCC9, ACTC1, ACTN2, BAG3, CASQ2, CHRM2, CRYAB, CSRP3, DES, DMD, DOLK, DSC2, DSG2, DSP, DTNA, EMD, GATAD1, GLA, JUP, LAMP2, LDB3, LMNA, MURC, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYOZ2, MYPN, NEBL, NEXN, PKP2, PLN, PRDM16, PRKAG2, PTPN11, RAF1, RBM20, RYR2, SCN5A, SGCD, TAZ, TCAP, TMEM43, TNNC1, TNNI3, TNNT2, TPM1, TRDN, TTN, TTR, VCL
- Next Generation Sequencing (copy number analysis included when data meets quality standards)
- Sanger Confirmation
7ml of whole blood (3–5ml for an infant) in a lavender top tube (K2EDTA or K3EDTA)
10 ug of DNA at a minimum concentration of 25 ng/ul (please provide DNA concentration)
81403 (1), 81404 (1), 81405 (12), 81406 (13), 81407 (4), 81408 (2), 81479 (1)
For questions, please contact us at 617-768-8500 or by email.