Triple Marker Test

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Understanding the Triple Marker Test

The Triple Marker Test, or Triple Screen Test, is a second-trimester non-invasive blood test usually performed between weeks 15 and 20 of pregnancy. This test screens for the risk of some chromosomal defects and neural tube defects in the unborn child.

Triple Marker Test Measures

The key components measured in this test include Alpha-fetoprotein (AFP), Human Chorionic Gonadotropin (hCG), and Estriol (uE3). AFP is a protein produced by the fetal liver, and abnormal levels may indicate neural tube defects or chromosomal disorders. hCG is a hormone produced by the placenta, and elevated levels can suggest an increased risk of Down syndrome. Estriol, an estrogen secreted by both the fetus and placenta, tends to be low in certain chromosomal disorders. By analyzing the levels of these substances, medical professionals can estimate the risk of specific fetal abnormalities, allowing for early diagnosis and timely intervention.

Triple Marker Test Price For Other Cities

Purpose and Significance of Triple Marker Test

Triple Marker Test is mainly done to evaluate the risk of:
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Frequently Asked Questions

Is the Triple Marker Test compulsory?

Is there any risk in taking the Triple Marker Test?

How accurate is the Triple Marker Test?

Will the Triple Marker Test detect all birth defects?

What can affect the test results?

Full Body Checkup Packages with Triple Marker Test in

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Full Body Checkup for Women - WellWise Exclusive Profile - Female

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  • Advance Cardiac Marker
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Medically Reviewed By
Dr. SANA ABEDIN
9+ Years of Experience
Last Updated :
May 19, 2025

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