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Pregnancy is a profound experience full of joy and responsibility. Maternal screening tests are critical for prenatal treatment since they provide important information about the fetus’s health and detect any issues early. This article describes the different types and relevance of maternal screening tests so you know what to expect throughout pregnancy.
Importance of Maternal Screening Tests
Maternal screening tests are necessary for:
Every pregnancy journey is unique and full of joy and excitement. Ensuring the baby’s healthy development and early detection of hazards is critical. The Double Marker Test, performed during the first trimester, is crucial in determining the risk of chromosomal abnormalities.
What is the Double Marker Test?
The Double Marker Test is a blood test performed between weeks 11 and 13 plus 6 days of pregnancy. It is frequently paired with a Nuchal Translucency (NT) scan to determine the risk of fetal chromosomal abnormalities.
Components of the Double Marker Test:
Purpose: These markers, along with the NT scan, help determine the risk of disorders, including Down syndrome (trisomy 21), Edwards syndrome (trisomy 18), and Patau syndrome (trisomy 13).
Procedure & Report Time: 2-3 ml blood sample is collected from the mother’s arm for the Double Marker test. During the procedure, relevant maternity details are documented. The sample is then processed in our advanced laboratory. The Double Marker test results are typically available within 2-3 working days, providing crucial insights for your prenatal care.
The first trimester Quadruple Marker Test is a crucial prenatal screening conducted early in pregnancy. Typically done between 12 weeks to 13 weeks and 6 days, this test helps assess the risk of chromosomal abnormalities and neural tube defects in the developing fetus. By providing valuable early information about the baby’s health, it allows expecting parents and healthcare providers to make informed decisions about further testing and care.
Why is the Quadruple Marker Test Done?
The primary reasons for conducting the Quadruple Marker Test are:
Procedure:
A 2-3 ml blood sample is drawn from the mother’s arm.
Report Time:
What is it?
The Quadruple Marker Test (or quad screen) is a second-trimester prenatal screening that determines the risk of chromosomal abnormalities and neural tube defects.
Why is it done?
The purpose of this test is to identify potential risks for Down syndrome, Edward syndrome, Patau syndrome (Trisomy 13), and neural tube problems such as spina bifida.
How it is done and its components:
Procedure:
A 2-3 ml blood sample is drawn from the mother’s arm.
Report Time:
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We are here to provide you with exceptional care and ensure you have a positive experience. Schedule your scan with us and take the next step toward better health today.
Prenatal Screening Test | When it is done (Gestational age) | Components |
Double Marker Test + NT (Nuchal Translucency) scan | 12 weeks to 13 weeks + 6 days (First trimester pregnancy) |
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First Trimester Quadruple Marker Test | 12 weeks to 13 weeks + 6 days (First trimester pregnancy) |
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Quadruple Marker Test | 15 to 20 weeks + 6 days (First trimester pregnancy) |
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Why Choose Our Services?
Get the Best in Maternity Care with Our Blood Tests!
Ensure your pregnancy journey is safe and informed with our comprehensive maternity blood tests at add-on Scans & Labs. Trust us for accurate results and expert care.
Book Your Test Today: Call or WhatsApp us at +91-9900811118 or visit our website to schedule your appointment. Experience exceptional care tailored to your needs!
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