Dilated Cardiomyopathy (DCM)

Introduction

We simultaneously sequence 23 genes known to cause inherited cardiomyopathy. We provide a comprehensive scientific interpretation of variants found and issue a report summarising our findings.

Referral information

For individuals with clinical features and investigations consistent with published criteria for familial DCM (European Heart Journal 1999;20:93-102). On identification of a pathogenic change in an index case presymptomatic testing of relatives can be offered. Referrals for testing are only accepted from a Consultant Cardiologist or a Consultant Clinical Geneticist (please contact the Clinical Genetics department for specific information). Referrals should be accompanied by a clinical diagnosis and details of family history. Referrals should also be accompanied by a completed standard referral form available in the Referral Forms section. For optimal results please send a fresh EDTA blood sample (1-4ml) or a minimum of 5µg of extracted DNA. For a full list of genes included in the assay please contact the laboratory.

Price & reporting times

Please contact the laboratory for prices.

Test	Price (NHS)	Price (non-NHS)	TRT
Dilated Cardiomyopathy (23 gene) panel	POA	POA	112cd
Bioinformatic Re-analysis	POA	POA

Test validation & quality assurance - information for users

The laboratory is UKAS assessed against ISO 15189 standards.

Sample requirements

4ml EDTA blood sample

Referral guidelines

Please see our referral guidelines for more information.

OMIM Number(s) - 601439, 102540, 102573, 600824, 125660, 603550, 150330, 600958, 160710, 160760, 613121, 172405, 613171, 600163, 601411, 604488, 188380, 191040, 191044, 191045, 191010, 188840, 193065

Gene(s) - ABCC9, ACTC1, ACTN2, CSRP3, DES, EYA4, LMNA, MYBPC3, MYH6, MYH7, NEXN, PLN, RBM20, SCN5A, SGCD, TCAP, TMPO, TNNC1, TNNI3, TNNT2, TPM1, TTN, VCL