Quadruple Marker Test
₹3,200.00 Original price was: ₹3,200.00.₹2,000.00Current price is: ₹2,000.00.
Quadruple Marker Test
- Required Blood Sample
₹3,200.00 Original price was: ₹3,200.00.₹2,000.00Current price is: ₹2,000.00.
Quadruple Marker Test
- Required Blood Sample
₹3,200.00 Original price was: ₹3,200.00.₹2,000.00Current price is: ₹2,000.00.
Test Instructions
- Required Blood Sample
- Description
The Quadruple Marker test (also known as the Quad Screen or Second Trimester Maternal Serum Screening) is a highly specialized prenatal blood diagnostic analysis performed during the second trimester of pregnancy. Rather than diagnosing a condition directly, this screening calculates the statistical probability or risk of a fetus having specific chromosomal abnormalities or structural birth defects. The test measures the exact concentrations of four essential substances traveling through the mother’s blood: Alpha-Fetoprotein (AFP), Human Chorionic Gonadotropin (hCG), Unconjugated Estriol (uE3), and Inhibin-A. Evaluating quadruple marker levels combines these biomarker counts with maternal parameters—such as precise gestational age, weight, and age—to provide comprehensive risk assessment scores. 🤰🧬 Screenings like this are crucial for helping parents and obstetricians make informed decisions regarding advanced prenatal care.
When is this test performed and for which diseases? 🤔
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To Evaluate Chromosomal Disorder Risks: This test is performed strictly between the 15th and 20th weeks of pregnancy (ideally during weeks 16-18) to screen for the statistical risk of Down Syndrome (Trisomy 21), a genetic condition that causes developmental and intellectual delays. 📊
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To Screen for Severe Structural Abnormalities: It is ordered during the second trimester to identify the likelihood of Neural Tube Defects (NTDs), such as Spina Bifida (incomplete closing of the spine) or Anencephaly (severe brain development defects), indicated primarily by elevated maternal AFP levels. 🧠🚨
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To Identify Edwards Syndrome Risks: This examination is performed to calculate the probability of Trisomy 18 (Edwards Syndrome), a severe chromosomal abnormality that causes profound developmental complications and multi-organ structural defects. 🔬
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To Detect Multi-Fetal Pregnancies: It is performed to cross-check clinical parameters, as altered marker patterns can sometimes indicate the presence of multiple gestations (twins or triplets) or help identify a miscalculated gestational age. 👶👶
Test Specifications: 📋
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Sample Type: Blood (Serum) 🩸 (Note: Accurate clinical data including the mother’s exact Date of Birth, current Weight, Diabetic status, and an updated Ultrasound/Acoustic scan showing fetal Crown-Rump Length or Biparietal Diameter must be provided alongside the sample).
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Preparation: No fasting is required; you can comfortably provide your blood sample at any time of the day. ☀️
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Reporting: Detailed statistical risk analysis charts utilizing specialized software (showing risk ratios like 1:250) are typically delivered within 48 to 72 hours. ⏱️
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