DOUBLE MARKER
Double Marker FMF approved is a prenatal screening test performed during the first trimester of pregnancy, typically between 9 to 13 weeks. The double marker FMF approved test measures two important biochemical markers in the mother’s blood free Beta hCG and PAPP-A (Pregnancy Associated Plasma Protein-A). These markers, when combined with ultrasound findings like NT scan, help assess the risk of chromosomal abnormalities such as Down syndrome (Trisomy 21), Trisomy 18, and Trisomy 13. The double marker FMF approved is especially valuable because it is approved by the Fetal Medicine Foundation (FMF), ensuring standardized and reliable risk assessment. The double marker FMF approved test does not diagnose conditions but provides a probability score to guide further testing if needed. Doctors often recommend double marker FMF approved test as part of routine antenatal care.
Sample
Serum
Fasting
Not required
Report
Within 24 hrs
Parameters
1
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CHANDAN DIAGNOSTICCC
₹2,520
Agilus Diagnostics
₹2,750
About the DOUBLE MARKER in Bareilly
Why is this test done?
The double marker FMF approved is crucial for early detection of potential chromosomal abnormalities. Early screening through the double marker FMF approved allows expecting parents and doctors to make informed decisions regarding further diagnostic procedures such as NIPT or amniocentesis. The double marker FMF approved is particularly important because it helps identify high-risk pregnancies early, enabling timely medical intervention and better pregnancy management. The double marker test is widely recommended as part of first trimester screening protocols globally. Key reasons: Early risk assessment of genetic conditions Helps plan further diagnostic tests Improves pregnancy monitoring Provides reassurance in low-risk cases Supports informed decision-making
How to prepare
No special preparation required.
Gender Eligibility
Female
Recommendations
All pregnant women (9–13 weeks) Women above 35 years IVF pregnancies Family history of genetic disorders Abnormal NT scan findings
Medical disclaimer: This information is for educational purposes only and is not a substitute for professional medical advice. Always consult a qualified doctor to interpret your reports.
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