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Double marker test result
Hcgb MoM 0.46 and Papp a Mom 0.38. All the three syndrome risk is mentioned as low. I'm worried about the Papp value. Is it very low? Please answer.
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How’s your nt scan need more details
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PAPP-A alone is not indicator for any chromosomal anomaly.Level 1 scan Nt-NB Scan is also done along with that.
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Level 2 scan done at 18-22 weeks for congenital anomalies and quadraple marker
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The screen result is the part that matters, and yours has come back low risk for all three conditions. Individual markers are not read on their own. The software combines your age, the nuchal translucency measurement, gestational age and both marker values, and a lower PAPP-A can be offset by the other inputs, which is what has happened here. A PAPP-A in this range with an otherwise low risk result does not indicate a chromosomal problem.
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Continue routine antenatal care and keep your anomaly scan at 18 to 22 weeks, which is the next real checkpoint. Share the full report with your obstetrician at your next visit so growth and blood pressure can be tracked.
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A lower PAPP-A is sometimes linked with placental function, so your doctor may watch fetal growth and blood pressure a little more closely. That is monitoring, not a diagnosis.
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Pls connect for online consultation and advice
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Dr. Pratibha P S
Gynecologist
10 yrs exp
Bangalore
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Dr. Neha Vashisth
Obstetrician
14 yrs exp
Jaipur
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Dr. Kinnari Amin
Gynecologist
14 yrs exp
Ahmedabad
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Dr. Shweta Lodhi Umate
Gynecologist
8 yrs exp
Nagpur
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Answer for the same
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Disclaimer : The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding your medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website.