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Double marker test variation
My first-trimester screening shows an elevated free β-hCG of 3.16 MoM, but the combined screening result for Trisomy 21 is 1:8625 and is reported as low risk. The NT scan was also reassuring, with NT 0.7 mm and the nasal bone visualized.
What would doctors generally recommend next in this situation—only a detailed fetal-medicine scan, or would NIPT also be advised?
Could this variation in the double-marker test cause any problems for the baby after delivery? Is there any increased risk of health or developmental problems after birth because of the elevated β-hCG, even though the overall screening result is low risk?
Answers (1)
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Ms. Shreya Mishra
Maternal and Fetal Medicine Specialist
1 yrs exp
Delhi
It will be better if u go for NIPT
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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.