🧪 What to Expect in a Double Marker Test Report? Explained by Dr. Shilpa G.B, Fertility & Pregnancy Specialist, Shanti Gynec Hospital The Double Marker Test helps assess the risk of genetic conditions like Down syndrome in early pregnancy (9–13 weeks). 🔍 The report includes: ✅ Free Beta-hCG – Higher levels may suggest increased risk. ✅ PAPP-A – Lower levels may indicate chromosomal issues. ✅ Risk Ratio for: Trisomy 21 (Down Syndrome) Trisomy 18 & 13 Example: 1 in 1000 (Low Risk) or 1 in 100 (H
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Understanding Genetic Tests During Pregnancy: Dual Marker, NT NB Scan, Quad Marker, and NIPT Today, let’s break down some important genetic screening tests and their significance during pregnancy. What Are These Tests? • Tests like Dual Marker, NT NB Scan, Quad Marker, and NIPT are designed to detect the probability of genetic syndromes, such as Down Syndrome or Edwards Syndrome, in the baby. • These are screening tests, not diagnostic tests. They assess risk ratios, such as: • “1 in 1 lakh chan
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Double marker is a blood test done between 11-14 weeks of gestation. THIS Test rule out chromosomal anomalies such as Down syndrome, this is only a screening test, and just give probabilities, One should go for Amniocentesis to confirm Down syndrome. #downsyndromeawareness #downsyndrome #chromosomal #chromosomalabnormality #doublemarker #doublemarkertest | Dr home - Dr shikha Agarwal
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