NGS Homologous Recombinant Deficiency HRR Panel Test
Cost: 10530.0 AED
Symptoms, Diagnosis, and Test Details
The NGS Homologous Recombinant Deficiency [HRR] Panel Test is a genetic test that analyzes specific genes involved in repairing DNA damage through a process called homologous recombination. This panel is used to identify mutations or alterations in genes that are associated with an increased risk of cancer, particularly breast and ovarian cancer.
The HRR panel typically includes genes such as BRCA1, BRCA2, PALB2, RAD51C, RAD51D, and ATM, among others. Mutations in these genes can impair the ability of cells to repair DNA damage, leading to an increased risk of cancer.
NGS, or next-generation sequencing, is a technology used to rapidly sequence large amounts of DNA in a single run. This allows for the simultaneous analysis of multiple genes, making it an efficient and cost-effective way to screen for genetic mutations associated with cancer risk.
The NGS HRR panel is typically recommended for individuals with a family history of breast or ovarian cancer, particularly if multiple family members have been diagnosed at a young age. It may also be recommended for individuals with a personal history of breast or ovarian cancer, as well as those with a history of other cancers associated with HRR gene mutations.
Test Information
- Test Name: NGS Homologous Recombinant Deficiency HRR Panel Test
- Components: EDTA Vacutainer (2ml)
- Price: 10530.0 AED
- Sample Condition: Peripheral blood + FFPE BLOCK
- Report Delivery: 4-6 weeks
- Method: NGS
- Test Type: Genetics
- Doctor: General Physician
- Test Department:
Pre Test Information
The NGS Homologous Recombinant Deficiency HRR Panel Test can be done with a doctor’s prescription. However, the prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.
Conclusion
The results of the NGS HRR panel can help guide personalized cancer risk management strategies, such as increased surveillance or prophylactic surgery, and may also inform treatment decisions for individuals with a cancer diagnosis.
Test Name | NGS Homologous Recombinant Deficiency HRR Panel Test |
---|---|
Components | EDTA Vacutainer (2ml) |
Price | 10530.0 AED |
Sample Condition | Peripheral blood + FFPE BLOCK |
Report Delivery | 4-6 weeks |
Method | NGS |
Test type | Genetics |
Doctor | General Physician |
Test Department: | |
Pre Test Information | NGS Homologous Recombinant Deficiency HRR] Panel can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad. |
Test Details |
The NGS Homologous Recombinant Deficiency [HRR] Panel is a genetic test that analyzes specific genes involved in repairing DNA damage through a process called homologous recombination. This panel is used to identify mutations or alterations in genes that are associated with an increased risk of cancer, particularly breast and ovarian cancer. The HRR panel typically includes genes such as BRCA1, BRCA2, PALB2, RAD51C, RAD51D, and ATM, among others. Mutations in these genes can impair the ability of cells to repair DNA damage, leading to an increased risk of cancer. NGS, or next-generation sequencing, is a technology used to rapidly sequence large amounts of DNA in a single run. This allows for the simultaneous analysis of multiple genes, making it an efficient and cost-effective way to screen for genetic mutations associated with cancer risk. The NGS HRR panel is typically recommended for individuals with a family history of breast or ovarian cancer, particularly if multiple family members have been diagnosed at a young age. It may also be recommended for individuals with a personal history of breast or ovarian cancer, as well as those with a history of other cancers associated with HRR gene mutations. The results of the NGS HRR panel can help guide personalized cancer risk management strategies, such as increased surveillance or prophylactic surgery, and may also inform treatment decisions for individuals with a cancer diagnosis. |