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Quadruple Marker with Graph - 2nd Trimester

Also referred as
Quadruple marker test
Quad marker screening
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For women
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4 tests
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₹3600
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A Quadruple Marker with Graph - 2nd Trimester test is the most common blood screening test done between the 14th and 22nd weeks (ideal 15-20 weeks, i.e., second trimester) of pregnancy to determine whether the baby is at risk for certain birth defects. It offers valuable information to ensure the well-being of both the mother and the unborn child.

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TATA 1mg Labs is a cutting-edge facility delivering top-quality diagnostic services right to your doorstep. We take pride in three core values: Assured Quality, Best Prices and Timely Reports. Transparency is at the heart of our operations, ensuring our customers always have clear and reliable information. Our dedicated team is committed to offering an exceptional customer experience and continually innovates to meet and exceed customer expectations.
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Understanding Quadruple Marker with Graph - 2nd Trimester

A Quadruple Marker with Graph - 2nd Trimester test is a prenatal screening test tailored to provide expectant parents with insights into the developing baby's health. It analyzes specific markers in the mother’s blood to assess the risk of chromosomal abnormalities, such as Down Syndrome (Trisomy 21) and Edwards Syndrome (Trisomy 18), wherein extra copies of chromosome 21 and 18 are present and affect the baby's physical and intellectual development. It also screens for neural tube defects like spina bifida (a spinal cord defect) and anencephaly (a brain defect). These birth defects can result in nerve damage, learning disabilities, paralysis, or stillbirth.

The Quad in Quadruple Marker with Graph - 2nd Trimester test refers to the four specific markers measured in the mother’s blood during the screening. These include Alpha-fetoprotein (AFP), Human Chorionic Gonadotropin (hCG), Estriol unconjugated (uE3), and Inhibin A. When assessed collectively, the levels of these markers help estimate the likelihood of certain fetal abnormalities that can affect the baby’s growth and development. Timely detection of these abnormalities is vital for ensuring comprehensive prenatal care and effectively addressing potential health problems. In addition to the traditional Quad marker analysis, the inclusion of a graphical representation enhances the interpretability of results. 

A Quadruple Marker with Graph - 2nd Trimester test is a screening test only; any abnormal result does not mean the unborn baby has a birth defect or genetic condition. It only tells whether the unborn baby is at risk of developing certain abnormalities, and further testing is required to confirm the diagnosis.

The recommendation of a Quadruple Marker with Graph - 2nd Trimester test is often based on maternal age, medical history, and individual risk factors for chromosomal abnormalities. Pregnant women should consult their doctor to determine the most appropriate screening or diagnostic test based on their specific circumstances. 

No special preparation is required before undergoing a Quadruple Marker with Graph - 2nd Trimester test. However, a woman needs to be prepared to provide informed consent before undertaking this test. The laboratory personnel will explain the purpose, benefits, and limitations of this test.

Abnormal lab test results represent only the risk but not the diagnostic outcomes. Increased risk does not mean the baby is affected; further tests must be performed before a confirmed diagnosis can be made. Talk to your doctor about your specific test results. 

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What does Quadruple Marker with Graph - 2nd Trimester measure?

Contains 4 tests

A Quadruple Marker with Graph - 2nd Trimester test measures the levels of four specific markers in a pregnant woman's blood. These markers are -Alpha-Fetoprotein (AFP), Human Chorionic Gonadotropin (hCG), Estriol Unconjugated , and  Inhibin-A.

The analysis of these four markers and other factors like maternal age and gestational age helps assess the risk of certain conditions in the developing baby. The graph in a Quadruple Marker with Graph - 2nd Trimester provides a visual representation of the levels of these markers during pregnancy. 

It is noteworthy that a Quadruple Marker with Graph - 2nd Trimester is a screening test, and any abnormal results may prompt further diagnostic testing for confirmation. Pregnant women should discuss their results and implications with their doctor.

The Inhibin A test measures the level of inhibin A in the blood. It is a hormone primarily produced by the ovaries in women. It plays a key role in regulating menstrual cycle and ovarian function by inhibiting the production of follicle-stimulating hormone (FSH). During pregnancy, elevated levels of Inhibin A may point towards a risk of certain chromosomal abnormalities like Down’s syndrome etc., in the fetus. 

The Inhibin A test is particularly useful in assessing ovarian function, fertility assessment, prenatal screening and diagnosing certain ovarian cancers.

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The HCG Beta Total Quantitative, Maternal test measures the levels of human chorionic gonadotropin (hCG) hormone in the blood. hCG is released in the blood during pregnancy and can be detected as early as 10 to 12 days after conception. The levels of this hormone gradually rise every 2 to 3 days (or 48 to 72 hours) and peak around 8 to 11 weeks after conception. After reaching the peak, the hCG levels decrease and remain steady for the rest of the pregnancy.

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An Alpha Feto Protein, Maternal test measures the amount of Alpha Fetoprotein in expectant mothers usually during the second trimester (14th and 22nd weeks). AFP is a protein produced by the fetus, primarily by the fetal liver and yolk sac, and it passes into the mother's blood. The test is typically performed to screen for certain fetal abnormalities, particularly neural tube defects (NTDs) such as spina bifida and anencephaly, as well as chromosomal abnormalities like Down syndrome (trisomy 21), Edwards syndrome (Trisomy 18), etc. 

Detecting these abnormalities early in pregnancy allows for appropriate medical management and intervention.

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The Estriol Unconjugated test is used to assess the level of unconjugated estriol (uE3) in the blood, a specific type of estrogen produced during the pregnancy phase. This hormone is mainly synthesized in the placenta and the fetus, with the fetus being responsible for a substantial amount of uE3 production as it grows. 

Monitoring the uE3 levels in the maternal serum is useful in evaluating the condition of the fetus. Abnormal unconjugated estriol levels may indicate pregnancy-related complications or concerns, including chromosomal abnormalities, fetal distress, or placental problems. The Estriol Unconjugated is particularly crucial in the second trimester to assess for some conditions, such as Down syndrome, Edward syndrome, or other chromosomal abnormalities, fetal growth and development. Hence the estriol unconjugated test is a significant part of prenatal care as it reveals information that may be valuable for the diagnosis and management of the mother and the baby.

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Quadruple Marker with Graph - 2nd Trimester test price for other cities

Price inNew DelhiRs. 3239
Price inBangaloreRs. 3019
Price inKolkataRs. 3149
Price inBhubaneshwarRs. 2850
Price inGhaziabadRs. 2850
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FAQs related to Quadruple Marker with Graph - 2nd Trimester

A Quadruple Marker with Graph - 2nd Trimester is a prenatal screening test that evaluates the risk of chromosomal abnormalities and neural tube defects in the developing baby, helping in early detection and appropriate management.
A quad marker test assesses four specific biomarkers: AFP (alpha-fetoprotein), HCG (human chorionic gonadotropin), Estriol (a form of estrogen), and Inhibin-A.
You can undergo a quad marker test in the second trimester, i.e., between weeks 15 and 22 of pregnancy.
The test involves a simple and safe blood draw from the pregnant woman, posing no risk to the developing baby. It is a non-invasive screening test.
A quad marker test primarily screens for Down syndrome (Trisomy 21) and Edwards’ syndrome (Trisomy 18).
No, this test is not specific to women aged 35 or older. It is recommended for all pregnant women, serving as an important test for detecting fetal abnormalities before birth. However, this test is highly recommended in women with risk factors like age of 35 or older, family history of birth defects, having a previous child with a birth defect, known type 1 diabetic woman, viral infection/ radiation exposure/ harmful drugs during pregnancy.
A normal quad marker test result (or a negative result) means the fetus is not at higher risk for a congenital disorder. It just means the risk is low but does not rule out other chromosomal defects like single-gene disorder or other complications.
The quad screen only checks your risk. It doesn’t tell if the developing baby has a genetic disorder. If your quad screen shows an increased risk for a congenital disorder, your doctor will suggest other tests like additional ultrasound or amniocentesis, which help determine if the fetus has a genetic disorder.
Down syndrome, or Trisomy 21, is a genetic disorder caused by the presence of an extra copy of chromosome 21. It can cause various physical and intellectual challenges.
Edwards’ syndrome, or Trisomy 18, is a rare genetic disorder resulting from an extra copy of chromosome 18. It manifests in distinctive physical abnormalities, including a small head, a small jaw, rocker bottom feet (a rounded sole on the bottom of the feet), etc.
Neural tube defects (NTDs), including spina bifida and anencephaly, are birth defects of the brain, spinal cord, and spine that occur due to abnormal neural tube development in the fetus. The diagnosis is made on maternal USG during pregnancy or by estimation of maternal serum alpha-fetoprotein (MSAFP) levels early in the second trimester (15–18 weeks of gestation).
References
  1. Greene ND, Copp AJ. Neural tube defects. Annu Rev Neurosci. 2014;37:221-42. [Accessed 20 Dec. 2023]. Available from:
  2. Screening for Down's syndrome, Edwards' syndrome and Patau's syndrome [Internet]. NHS; 19 April 2021 [Accessed 20 Dec. 2023]. Available from:
  3. Sablok A, Sharma A, Ahmed CS, Kaul A. Performance of second-trimester maternal biochemistry screening (quadruple test vs. triple test) for trisomy 21: An Indian experience. Indian J Med Res. 2021 May;154(5):716-722. [Accessed 20 Dec. 2023]. Available from:
  4. Gordon S, Umandap C, Langaker MD. Prenatal Genetic Screening. [Updated 2023 Jan 16]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2023 Jan-. Available from:
  5. Güdücü N, Görmüş U, Güner Eİ, Güzel O, Kavak ZN. Quadruple test parameters in art pregnancies. Int J Clin Exp Med. 2014 Aug 15;7(8):2319-23. PMID: 25232428; PMCID: PMC4161588. [Accessed 20 Dec. 2023]. Available from:
  6. Commit to Healthy Choices to Help Prevent Birth Defects [Internet]. CDC; 28 June 2023 [Accessed 20 Dec. 2023]. Available from:
  7. Institute of Medicine (US) Committee on Improving Birth Outcomes; Bale JR, Stoll BJ, Lucas AO, editors. Reducing Birth Defects: Meeting the Challenge in the Developing World. Washington (DC): National Academies Press (US); 2003. 3, Interventions to Reduce the Impact of Birth Defects. [Accessed 20 Dec. 2023]. Available from:
  8. Boonpiam R, Wanapirak C, Sirichotiyakul S, Sekararithi R, Traisrisilp K, Tongsong T. Quad test for fetal aneuploidy screening as a predictor of small-for-gestational age fetuses: a population-based study. BMC Pregnancy Childbirth. 2020 Oct 15;20(1):621. [Accessed 20 Dec. 2023]. Available from:
Recommended for women
This package is designed with women's health considerations in mind, offering targeted assessments to address unique wellness needs and potential risks.
Contains 4 tests
Inhibin A
HCG Beta Total Quantitative, Maternal
Alpha Feto Protein, Maternal
Estriol Unconjugated
Report delivery
Standard time
48 hrs
For slots after 11 AM, report will be delivered in 72 hours.
Samples required
Blood
Our phlebotomist will draw a blood sample, typically from a vein in your inner elbow.
Preparations
1
Provide maternal Date of birth (dd/mm/yy); Date of the first day of the last menstrual period (LMP), Ultrasound, Number of Fetuses (Single/Twins); Diabetic status and Body Weight in Kg, IVF, Smoking & Previous history of Trisomy 21 pregnancy at the time of sample collection.
2
A duly filled Maternal Serum Screen requisition form (Annexure - CR/02) is mandatory. Valid between 14-22 weeks gestation (Ideal 15-20 weeks). USG report is required.
Why is this test booked?
1
To assess the risk of certain chromosomal abnormalities in the developing baby.
2
To assess the risk of Down Syndrome (Trisomy 21) in the developing baby.
3
To assess the risk of Edwards Syndrome (Trisomy 18) in the developing baby.
4
To assess the risk of neural tube defects like spina bifida in the developing baby.
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