PreSENTIA Hereditary Cancer Test by Medicover (62 genes)
The PreSENTIA Hereditary Cancer Test is a comprehensive test that includes screening of germline mutations in 62 genes.Mutations in the genes tested have been linked to cancer development. The Pan-Cancer panel also screens for germline mutations associated with 24 different predisposing cancer syndromes including breast cancer, ovarian cancer and Lynch Syndrome. Identifying germline mutations associated with cancer susceptibility empowers healthcare providers and patients, as it allows them to take better and more informed decisions. The test can be done on a home saliva test without the need for a blood sample.
Who is this test for?
You should get tested if you meet at least one of the criteria below:
• You have a personal or family history of a hereditary cancer syndrome
• You have been diagnosed with a type of cancer before the age of 50
• You have several family members on the same side of the family with cancer
• You have family members with early cancer onset
• You have family members with rare cancer types
• You have family members with an unusual type of cancer (breast cancer in a male)
• You have a family member that has been diagnosed with a germline mutation associated with cancer susceptibility
• You have history of previous malignancies
• You belong in specific ancestry groups who have high risk for developing specific types of cancer (e.g Ashkenazi Jewish who have high risk developing breast or prostate cancer)
How many genes are tested in the Presentia Hereditary Cancer Test?
62 genes
Cancer syndromes are associated with the Presentia Hereditary Cancer Test?
24 Hereditary cancer syndromes are associated with this panel. These are:
• Ataxia-telangiectasia syndrome (ATM)
• BAP1 mutation associated disease (BAP1)
• Constitutional mismatch repair syndrome (EPCAM, MSH2, MSH6, MLH1, PMS2)
• DICER 1 syndrome (DICER1)
• Familial Adenomatous Polyposis / Attenuated Familial Adenomatous Polyposis (APC)
• Fanconi anemia syndrome (FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, SLX4, ERCC4, BRCA1, BRCA2, BRIP1, PALB2, RAD51C)
• Hereditary breast cancer and ovarian cancer syndrome (BRCA1, BRCA2)
• Hereditary diffuse gastric syndrome (CDH1)
• Hereditary mixed polyposis syndrome (GREM1)
• Hereditary melanoma-pancreatic cancer syndrome (CDKN2A, CDK4)
• Hereditary Paraganglioma – Pheochromocytoma syndrome (SDHD, SDHAF2, SDHC, SDHB)
• Juvenile polyposis syndrome (SMAD4, BMPR1A)
• Li-Fraumeni syndrome (TP53)
• Li-Fraumeni syndrome 2 (CHEK2)
• Lynch syndrome (EPCAM, MLH1, MSH2, MSH6, PMS2)
• Multiple endocrine neoplasia type 1 (MEN1)
• Multiple endocrine neoplasia type 2 (RET)
• MUTYH-associated polyposis syndrome (MUTYH)
• Peutz-Jeghers syndrome (STK11)
• Polymerase proofreading associated syndrome (POLD1, POLE)
• PTEN hamartoma syndrome (PTEN)
• Retinoblastoma (RB1)
• Von-Hippel Lindau syndrome (VHL)
• Xeroderma Pigmentosum syndrome (DDB2, ERCC1, ERCC2, ERCC3, ERCC4, ERCC5, POLH, XPA, XPC)
References and more information:
- The above information was taken by professional bodies such as NCCN, American Cancer society and National Cancer Institute
- Click here to read more about Understanding Hereditary Cancer
