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Breast Comprehensive Panel NGS Genetic Test Cost

Original price was: 6,000 د.إ.Current price is: 4,400 د.إ.

-27%

The Breast Comprehensive Panel NGS (Next-Generation Sequencing) Genetic Test is a cutting-edge diagnostic tool offered by DNA Labs UAE, designed to provide an in-depth analysis of genetic mutations associated with breast cancer. Priced at 4400 AED, this comprehensive test screens for a wide array of genetic markers that are known to influence the risk of developing breast cancer. Utilizing the latest NGS technology, the panel can simultaneously analyze multiple genes to detect mutations with high accuracy and speed, enabling personalized risk assessment and guiding targeted treatment options. This test is especially valuable for individuals with a family history of breast cancer or those seeking to understand their genetic predisposition to the disease. By providing detailed genetic insights, the Breast Comprehensive Panel NGS Genetic Test empowers patients and healthcare providers to make informed decisions regarding prevention, surveillance, and management strategies for breast cancer.

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Breast Comprehensive Panel NGS Genetic Test Price 4400 AED

Navigating Your Health: An Insight into the Breast Comprehensive Panel NGS Genetic Test in the UAE

Breast cancer is a significant health issue for many women in the UAE. The Breast Comprehensive Panel Next-Generation Sequencing (NGS) Genetic Test serves as an essential resource for those who wish to proactively assess their personal risk of developing breast cancer.

Decoding the NGS Test: Unveiling Your Genetic Profile

Our genes are the architects of our physical attributes and health. NGS technology enables scientists to examine a large segment of your genes at once. The Breast Comprehensive Panel NGS Genetic Test is designed to target genes linked with a heightened risk of developing breast cancer.

Why Opt for the Breast Comprehensive Panel NGS Genetic Test?

Knowledge Empowers: This test equips you with crucial information about your genetic susceptibility to breast cancer, enabling you to make educated health decisions in consultation with your doctor. Early Detection Leads to Improved Prognosis: Recognizing a genetic risk factor for breast cancer facilitates earlier detection through regular screenings and potential risk-mitigation strategies, significantly enhancing treatment outcomes and overall prognosis. Considerations for Family Planning: If breast cancer runs in your family, this test can ascertain if you possess genes that could be inherited by your children. This information is invaluable for genetic counseling and family planning discussions.

Advantages of the Breast Comprehensive Panel NGS Genetic Test in the UAE:

Cutting-Edge Technology: NGS provides a more thorough analysis than conventional genetic testing methods, potentially uncovering a wider array of potential risk factors. Proactive Stance: This test enables you to adopt a proactive stance towards your breast health, facilitating early intervention and preventive actions. Peace of Mind: Understanding your genetic composition can offer peace of mind or stimulate further conversations with your doctor to devise a personalized healthcare strategy.

Who Stands to Gain from the Breast Comprehensive Panel NGS Genetic Test? T

his test is particularly beneficial for women who have: A family history of breast cancer, particularly in immediate relatives (mother, sister, daughter) A personal history of specific benign breast conditions Worries about their inherited risk of breast cancer

What Does the Test Involve?

The Breast Comprehensive Panel NGS Genetic Test typically requires a straightforward blood draw. There’s generally no special preparation needed.

Interpreting the Results and Future Course of Action:

A genetic counselor will decode your test results and elucidate their implications for your breast cancer risk. The results may suggest:

Negative Result: This signifies no detected genetic mutations linked with a high risk of breast cancer. However, routine screenings are still advised. Positive Result: A positive result doesn’t assure you will develop breast cancer, but it does suggest a higher risk. Your doctor will discuss personalized risk-reduction strategies such as increased screening frequency, preventive medications, or potential lifestyle changes.

The Importance of Genetic Counseling:

It’s highly recommended to consult a genetic counselor before and after the test. The counselor can elaborate on the test, address any concerns you might have, and guide you through the implications of the results for your unique situation.

Taking the Reins of Your Breast Health

If you’re apprehensive about your risk of breast cancer, discussing the Breast Comprehensive Panel NGS Genetic Test with your doctor in the UAE can be a pivotal move towards a proactive approach to your health. Early detection and knowledge are potent weapons in the battle against breast cancer.

Test Cost:

AED 4400.0

Test Name

Breast Comprehensive Panel NGS Genetic DNA Test

Components

Sample Condition

Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery

3 to 4 Weeks

Method

NGS Technology

Test Type

Cancer

Doctor

Oncologist

Test Department

Genetics

Pre Test Information

Clinical History of Patient who is going for Breast Comprehensive Panel NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ABRAXAS1, ATM, BARD1, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, DICER1, EPCAM, FANCC, MEN1, MLH1, MRE11, MSH2, MSH6, MUTYH, NBN, PALB2, PMS1, PMS2, PTEN, RAD50, RAD51C, RAD51D, RECQL, SMARCA4, STK11, TP53, XRCC2

Test Details

Breast comprehensive panel NGS genetic DNA test is a type of genetic test that analyzes specific genes associated with breast cancer. This panel test uses next-generation sequencing (NGS) technology to examine multiple genes simultaneously, providing a more comprehensive analysis than traditional single-gene tests.

The breast comprehensive panel NGS genetic DNA test can identify mutations in genes such as BRCA1 and BRCA2, which are associated with an increased risk of developing breast and ovarian cancer. Other genes analyzed in this panel may include ATM, BARD1, BRIP1, CDH1, CHEK2, NBN, PALB2, RAD51C, and RAD51D.

This test is typically recommended for individuals with a personal or family history of breast cancer, particularly if there are multiple cases of breast or ovarian cancer in the family, early onset of breast cancer, or male breast cancer. The results of this test can help inform medical management decisions, such as increased surveillance or risk-reducing surgeries.

It is important to note that not all genetic mutations identified by this test are definitively associated with an increased risk of breast cancer, and the interpretation of test results should be done in consultation with a healthcare provider trained in genetics.

Test NameBreast comprehensive panel NGS Genetic DNA Test
Components
Price4400.0 AED
Sample ConditionBlood or Extracted DNA or One drop Blood on FTA Card
Report Delivery3 to 4 Weeks
MethodNGS Technology
Test typeCancer
DoctorOncologist
Test Department:Genetics
Pre Test InformationClinical History of Patient who is going for Breast comprehensive panel NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ABRAXAS1, ATM, BARD1, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, DICER1, EPCAM, FANCC, MEN1, MLH1, MRE11, MSH2, MSH6, MUTYH, NBN, PALB2, PMS1, PMS2, PTEN, RAD50, RAD51C, RAD51D, RECQL, SMARCA4, STK11, TP53, XRCC2
Test DetailsBreast comprehensive panel NGS genetic DNA test is a type of genetic test that analyzes specific genes associated with breast cancer. This panel test uses next-generation sequencing (NGS) technology to examine multiple genes simultaneously, providing a more comprehensive analysis than traditional single-gene tests.

The breast comprehensive panel NGS genetic DNA test can identify mutations in genes such as BRCA1 and BRCA2, which are associated with an increased risk of developing breast and ovarian cancer. Other genes analyzed in this panel may include ATM, BARD1, BRIP1, CDH1, CHEK2, NBN, PALB2, RAD51C, and RAD51D.

This test is typically recommended for individuals with a personal or family history of breast cancer, particularly if there are multiple cases of breast or ovarian cancer in the family, early onset of breast cancer, or male breast cancer. The results of this test can help inform medical management decisions, such as increased surveillance or risk-reducing surgeries.

It is important to note that not all genetic mutations identified by this test are definitively associated with an increased risk of breast cancer, and the interpretation of test results should be done in consultation with a healthcare provider trained in genetics.