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Cancer is preventable and treatable with early diagnosis. Although cancer is mostly the result of mutations that accumulate over a lifetime, a significant proportion of it is inherited. This means that if a blood relative has cancer, you may be a carrier. To find out this risk, it is possible to examine cancer risk genes identified in scientific articles and medical protocols. With the new generation sequencing technology of familial cancer screening, a tube of blood is enough to get this information. Hereditary Cancer Panels are used for this process.

Test Adıİncelenen Bölgeler
Comprehensive Hereditary Cancer Panel523 gene DNA SNVs, small in/dels, 59 CNV amp/dels, 23 Translocations
Comprehensive Hereditary Breast and Ovarian Cancer PanelATM, BARD1, BRIP1, CDH1, CHEK2, NBN, PALB2, PTEN, RAD51C, RAD51D, STK11, TP53,BRCA1,BRCA2
Comprehensive Inherited Colorectal Cancer PanelAPC, MUTYH, MLH1, MSH2, MSH6, PMS1, PMS2, EPCAM, BMPR1A, SMAD4, STK11, PTEN, TP53, AXIN2, CDH1, CHEK2, GREM1, MSH3, NTHL1, POLD1, POLE
Hereditary Breast and Ovarian Cancer PanelBRCA1, BRCA2 & MPLA
Hereditary Colorectal Cancer BiomarkerMLH1