Understanding the Double Marker Test: A Must for Expecting Moms
Discover the importance of the Double Marker Test for expecting moms. Learn how it helps detect key pregnancy health markers.

Pregnancy is one of the most beautiful journeys in a woman’s life. It’s a time filled with excitement, hope, and countless dreams. But along with all the joy, there are also a few important responsibilities — especially when it comes to the health of the baby. One of those responsibilities includes undergoing the right prenatal tests. Among them, the Double Marker Test in Chandigarh is gaining a lot of attention for all the right reasons.
So, if you're an expecting mom or planning to be one soon, this guide will walk you through what the double marker test is, why it matters, and how it helps ensure a safer pregnancy.
What is the Double Marker Test?
The Double Marker Test is a type of prenatal screening test that helps assess the risk of chromosomal abnormalities in a developing fetus — especially Down syndrome, Trisomy 18, and Trisomy 21. It's usually recommended during the first trimester (between the 10th and 14th weeks of pregnancy).
This test checks for two specific substances in the mother’s blood:
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Free Beta hCG (Human Chorionic Gonadotropin)
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PAPP-A (Pregnancy-Associated Plasma Protein-A)
When combined with an ultrasound report (NT scan), the results offer insights into how the pregnancy is progressing.
Why is This Test Important?
The earlier you know about potential health risks, the better your doctor can guide you on next steps. Here’s why the double marker test is so useful:
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Early Detection: It helps identify any risk of genetic or chromosomal abnormalities.
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Peace of Mind: If the results are normal, it gives expecting parents a sense of reassurance.
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Better Planning: If the test results suggest a higher risk, doctors can advise further diagnostic tests like NIPT or amniocentesis.
Who Should Take the Double Marker Test?
Though it’s mostly offered to all pregnant women, your doctor might strongly recommend it if:
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You're above the age of 35
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You have a family history of genetic disorders
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You've had a previous pregnancy with abnormalities
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You’ve had multiple miscarriages in the past
When and How is the Test Done?
The ideal time for a double marker test is between 10 and 14 weeks of pregnancy. The process is simple:
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A small blood sample is collected from the mother.
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The results are calculated by combining the blood test data with findings from the NT scan.
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The risk is then calculated using various factors such as the mother’s age, gestational age, and hormone levels.
It’s a non-invasive and safe procedure for both mother and baby.
Understanding the Results
The test does not confirm whether your baby has a genetic condition. Instead, it shows whether your baby might be at higher or lower risk. The results are usually categorized into:
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Screen Negative (Low Risk): This means everything seems fine.
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Screen Positive (High Risk): This doesn’t mean there’s definitely a problem, but more tests may be needed.
Remember, a high-risk result is not a diagnosis. It only signals the need for further evaluation.
Advantages of the Double Marker Test
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Non-invasive and safe
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Quick and painless
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Provides early warnings
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Helps avoid unnecessary stress later in pregnancy
Common Myths Around the Test
Myth 1: “It’s only for older pregnant women.”
Fact: While age can increase risk, this test is useful for women of all ages.
Myth 2: “Positive result means my baby has a problem.”
Fact: A positive (or high-risk) result just suggests a chance — not a certainty.
Myth 3: “It can harm the baby.”
Fact: Not true. It’s just a simple blood test and completely safe.
Why Choose the Right Centre?
Accuracy is key when it comes to prenatal tests. The quality of the test depends a lot on the technology used and expertise of the diagnostic centre. That’s why choosing a trusted name like The Garbh can make a real difference in how your pregnancy journey goes.
They not only provide accurate testing but also give proper guidance and emotional support — which is just as important.
A Word from Experts
Doctors usually recommend pairing the double marker test with the NT scan for better accuracy. If both results are normal, it reduces the need for further invasive tests.
However, if the result is not what you expected, don’t panic. Just speak to your gynecologist or a genetic counselor. They’ll help you understand what it means and what to do next.
Final Thoughts
Pregnancy is an emotional ride, and every parent wants to do everything they can to ensure their baby is healthy. The double marker test is a small but powerful step toward that goal. It offers valuable insight and helps you make informed decisions early in pregnancy.
If you're based in or around Chandigarh and considering prenatal screening, don’t forget to explore the Dual Marker Test in Chandigarh through trusted labs like The Garbh. Their experienced team and modern technology ensure that you're in safe hands — right from the very start of your journey into parenthood.
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