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Double Marker Test

870 د.إ

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The Double Marker Test is a crucial prenatal screening conducted during the first trimester of pregnancy, specifically between the 10th and 13th weeks. This test is designed to evaluate the risk of the fetus developing chromosomal abnormalities, such as Down syndrome (Trisomy 21) and Edward syndrome (Trisomy 18). It measures the levels of two specific markers in the mother’s blood: Free Beta-hCG (human chorionic gonadotropin) and PAPP-A (Pregnancy Associated Plasma Protein-A). The results, combined with the mother’s age and the nuchal translucency measurement from an ultrasound, help in assessing the risk of chromosomal abnormalities in the fetus.

In the UAE, the Double Marker Test is available at DNA Labs UAE, a reputable facility known for its advanced diagnostic services. The cost of the test at DNA Labs UAE is 870 AED. Opting for this test at DNA Labs ensures that expectant parents receive accurate and reliable screening results, which are crucial for making informed decisions about the pregnancy.

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  • This test is not intended for medical diagnosis or treatment
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Double Marker Test Cost AED:870.0

Overview

The double marker test is a prenatal screening test that is performed during the first trimester of pregnancy. It involves measuring two specific substances in the mother’s blood: beta-human chorionic gonadotropin (-hCG) and pregnancy-associated plasma protein-A (PAPP-A). This test is primarily used to screen for chromosomal abnormalities in the fetus, particularly Down syndrome (trisomy 21) and Edwards syndrome (trisomy 18). It helps in assessing the risk of these conditions in the early stages of pregnancy.

Test Details

The double marker test is usually done between 10 and 13 weeks of pregnancy and involves a blood sample taken from the mother. The results of the test, along with other factors such as the mother’s age, are used to calculate the risk of the fetus having a chromosomal abnormality. If the double marker test shows an increased risk, further diagnostic tests such as amniocentesis or chorionic villus sampling may be recommended to confirm the diagnosis.

Pre Test Information

The double marker test can be done with a doctor’s prescription. However, it is not applicable for surgery and pregnancy cases or people planning to travel abroad.

Cost and Report Delivery

The cost of the double marker test at DNA Labs UAE is AED 870.0. The report is typically delivered within 2-3 days.

Method and Test Type

The double marker test at DNA Labs UAE is performed using the Chemilumicent Immunoassay method. It falls under the category of genetics tests.

Doctor and Test Department

The double marker test is conducted by doctors specializing in oncology. It is performed in the test department of DNA Labs UAE.

Risks and Limitations

The double marker test is generally considered safe, but like any medical procedure, it may have some risks and limitations. It is important to discuss the benefits, risks, and limitations of the test with a healthcare provider before undergoing the test.

For more information or to schedule an appointment, please contact DNA Labs UAE.

Test Name Double Marker Test
Components Plain (1-2ml)
Price 870.0 AED
Sample Condition Serum
Report Delivery 2-3 days
Method Chemilumicent Immunoassay
Test type Genetics
Doctor Oncology
Test Department:
Pre Test Information Double Marker can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad.
Test Details

Double marker test is a prenatal screening test that is performed during the first trimester of pregnancy. It involves measuring two specific substances in the mother’s blood: beta-human chorionic gonadotropin (-hCG) and pregnancy-associated plasma protein-A (PAPP-A).

The double marker test is primarily used to screen for chromosomal abnormalities in the fetus, particularly Down syndrome (trisomy 21) and Edwards syndrome (trisomy 18). It helps in assessing the risk of these conditions in the early stages of pregnancy.

The test is usually done between 10 and 13 weeks of pregnancy and involves a blood sample taken from the mother. The results of the test, along with other factors such as the mother’s age, are used to calculate the risk of the fetus having a chromosomal abnormality.

If the double marker test shows an increased risk, further diagnostic tests such as amniocentesis or chorionic villus sampling may be recommended to confirm the diagnosis.

It is important to note that the double marker test is a screening test and not a diagnostic test. It helps in identifying women who may be at a higher risk of having a baby with a chromosomal abnormality, but it cannot provide a definitive diagnosis.

The double marker test is generally considered safe, but like any medical procedure, it may have some risks and limitations. It is important to discuss the benefits, risks, and limitations of the test with a healthcare provider before undergoing the test.

SKU: TEST-5948 Category:

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