Carrier Screening Test sale cost 11400 AED
Clinical Exome Trio Sequencing Test sale cost 12000 AED Clinical Exome Trio Sequencing Test 15,000 د.إ 12,000 د.إ
Sale!

Carrier Screening Test

11,400 د.إ

-25%

Carrier screening tests are genetic tests designed to determine whether an individual is a carrier of specific genetic disorders. These tests are particularly important for couples planning to have children, as they can help identify the risk of passing on genetic conditions to their offspring. The carrier screening test at DNA Labs UAE is comprehensive, offering insights into a wide array of genetic disorders that could potentially affect future generations.

The cost of the carrier screening test at DNA Labs UAE is 11,400 AED. This investment allows prospective parents to make informed decisions about their family planning, armed with knowledge about their genetic makeup and potential risks. The testing process involves collecting a small sample of DNA, typically through a blood draw or a cheek swab, which is then analyzed in the lab for genetic markers associated with various inherited conditions.

DNA Labs UAE utilizes advanced genetic testing technologies to provide accurate and reliable results. The screening covers a broad spectrum of genetic disorders, ensuring that individuals have a comprehensive understanding of their carrier status. With this information, couples can seek genetic counseling and consider their options for family planning with greater confidence and peace of mind.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

Carrier Screening Test

At DNA Labs UAE, we offer the Carrier Screening Test to help identify whether a person is a carrier of a genetic disorder. This test is crucial for couples who are planning to have a child, as it helps determine the risk of having a child with a genetic disorder.

Test Name: Carrier Screening Test

Components: DNA analysis for specific genetic mutations

Price: 11400.0 AED

Sample Condition: Blood

Report Delivery Method: Test results will be provided by a doctor

Test Type: Genetic test

Test Department: DNA Labs UAE

Pre Test Information

Carrier screening is typically performed before pregnancy to identify couples who are at risk of having a child with a genetic disorder. It is important to undergo this test as carriers do not show any symptoms of the disorder, making it difficult to detect without testing.

Test Details

Carrier screening involves taking a blood sample or a sample of saliva and analyzing the DNA for specific genetic mutations. The most common genetic disorders screened for include cystic fibrosis, sickle cell anemia, Tay-Sachs disease, and thalassemia.

If both partners are carriers of the same genetic disorder, there is a 25% chance that their child will inherit two copies of the mutated gene and develop the disorder. Identifying carriers allows couples to make informed decisions about their reproductive options.

Couples who are identified as carriers of a genetic disorder can choose to undergo additional testing, such as pre-implantation genetic diagnosis or prenatal testing, to determine the risk of having an affected child.

By offering the Carrier Screening Test, DNA Labs UAE aims to provide couples with the necessary information to make informed decisions about their family planning. Our team of experts is dedicated to delivering accurate and reliable test results.

Test Name Carrier Screening Test
Components
Price 11400.0 AED
Sample Condition Blood
Report Delivery
Method
Test type
Doctor
Test Department:
Pre Test Information
Test Details

Carrier screening is a genetic test that identifies whether a person is a carrier of a genetic disorder. A carrier is a person who has one copy of a gene mutation that causes a genetic disorder but does not show any symptoms of the disorder. Carrier screening is usually done before pregnancy to identify couples who are at risk of having a child with a genetic disorder. The test is done by taking a blood sample or a sample of saliva and analyzing the DNA for specific genetic mutations. The most common genetic disorders screened for include cystic fibrosis, sickle cell anemia, Tay-Sachs disease, and thalassemia. If both partners are carriers of the same genetic disorder, there is a 25% chance that their child will inherit two copies of the mutated gene and develop the disorder. Couples who are identified as carriers of a genetic disorder can choose to undergo additional testing, such as pre-implantation genetic diagnosis or prenatal testing, to determine the risk of having an affected child.

SKU: TEST-685 Category:

Related products