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Double Marker Test in Amritsar

Also called: Maternal serum screening, First trimester screening, Dual marker test

SAMPLE
Blood
Report
Same or next day
PREPARATIONS
No special preparation

The test at a glance

What it checks
Double Marker Test test is a clinically significant diagnostic investigation used to evaluate, screen, or monitor underlying health conditions. It provides actionable insights that support early diagnosis, treatment planning, and long-term disease management.
Report delivery
Sample before 12 PM → by 8:30 PM today | Sample after 12 PM → by 1 PM tomorrow
Test for
Women, Family
Age group
All Ages
Commonly advised for
Developmental delay, seizures, low muscle tone

What is a Double Marker Test ?

Know More About This Test

The Double Marker Test is a prenatal screening test performed in the first trimester (11–14 weeks) of pregnancy. It measures two biochemical markers—free β-hCG and PAPP-A—to assess the risk of chromosomal abnormalities such as Down syndrome (Trisomy 21) and Trisomy 18.

This test is often combined with nuchal translucency (NT) ultrasound for greater accuracy.

Why Is This Test Recommended?

  • Early prenatal risk assessment
  • Screen for chromosomal abnormalities
  • Guide need for advanced diagnostic testing
  • Reassure low-risk pregnancies

Understanding the Double Marker Test

Abnormal marker levels do not confirm a disorder but indicate increased risk, prompting further diagnostic tests like NIPT or amniocentesis.

Who Should Take This Test?

  • All pregnant women
  • Women above 30–35 years
  • High-risk pregnancies

Preparation

  • No fasting required
  • Accurate gestational age essential

Results Interpretation

  • Low risk: No further testing needed
  • High risk: Diagnostic tests advised

FAQs

  • Is it mandatory? No, the Double Marker Test is recommended but optional, particularly for women over 35 or those with risk factors, as it provides valuable early insights without being required for all pregnancies.
  • Is it diagnostic? No, it is a screening test only and does not diagnose chromosomal abnormalities definitively; it calculates risk levels based on marker measurements, with high-risk results leading to confirmatory tests like amniocentesis.
  • Can it harm the fetus? No, the Double Marker Test is completely safe and non-invasive, involving only a simple blood draw from the mother with no risk to the fetus or pregnancy.
  • What if results are high risk? If results indicate high risk, further diagnostic tests such as non-invasive prenatal testing (NIPT), chorionic villus sampling (CVS), or amniocentesis are advised to confirm the findings and discuss options with a genetic counselor.
  • Is ultrasound required? Yes, ultrasound is required for optimal accuracy, as it measures nuchal translucency alongside the blood markers to provide a combined risk assessment that's more reliable than blood tests alone.

Who should take this test

The Double Marker Test is a first-trimester screening test done in pregnancy at a specific week. It is meant for:

  • Pregnant women whose doctor has advised first-trimester screening
  • Women who want a risk assessment for certain chromosomal conditions
  • Women with a relevant family or medical history, as advised by their doctor

Double Marker Test testing in Amritsar

Tapadia Diagnostic Centre in Amritsar offers NABL-accredited Double Marker Test test from a Blood sample(s). Maternal serum screening, First trimester screening, Dual marker test is also prescribed for Developmental delay, seizures, low muscle tone. Established in 1989, this doctor-led diagnostic centre ensures high accuracy. Home sample collection and walk-in facility available at our Amritsar center. Pay at the centre with no advance payment. Book online or visit us.

Frequently asked questions

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Centers You Can Choose To Visit

Double Marker Test in Amritsar

Rated 4.6 on Google From 6,477 patient reviews across our Hyderabad centres.

Every report, kept for you Past reports stay in your account and can be downloaded again.

NABL accredited Every result reviewed by a qualified pathologist before it reaches you.

Four decades of practice A family-run diagnostic centre, trusted by doctors and households since 1989

Medically Reviewed by Qualified Biochemists

Male and female doctors standing together in a clinic.
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