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NT value 3.2 mm
My NT value in 13 week is 3.2 mm. I have done NIPT and Aminocintesis. Both report came back as normal. So will my baby be ok?
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Ok No worries NIPT test is correct
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You have got your NIPT done too soon. NIPT is ideally done at about 18 weeks . In any case the highest sensitivity of NIPT is 99.9% . So there are only that many chances of the baby being normal.
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If NIPT and amniocentesis are normal then chances of structural congenital anomalies are low as they are more specific tests,recommended early anomaly scan around 16/17weeks.
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No chromosomal abnormality if amniocentesis is normal.but you need TIFFA  at 18 to 20 weeks to rule out structural anomalies
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These tests are normal.Go for triple marker and level 2 scan at 18 to 20 wk of pregnancy to rule out congenital anomalies.
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Pls connect for online consultation and advice
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NIPT and amniocentesis are definitive test means more accurate test to detect abnormality in the baby.Since they have come normal there is very less chance of any abnormality.
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Anamoly scan to be done between 18-22 weeks
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Get done anomaly scan at 18 weeks and also on 22 weeks
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For structural anomalies , get your early tiffa and late tiffa
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If nipt and amniocentesis are normal, nothing to worry, early anomaly scan at 18 weeks and repeat anomaly scan at 22 weeks
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Anomaly scan at 18-20 weeks These seem to be normal
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At 13 weeks we have NT - NB , NIPT normally , if both are normal then possibility of structural defect are very low , but still to be on safer side get TIFFA at 18-20 weeks and 2D echo at 22 weeks And don’t take stress
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NT - raised borderline Nipt if its normal -it rules out down syndrome by 99% For structural abnormalities get an anomaly scan around 18 weeks
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At present nothing more needs to be done. Get a level 2 scan at 18-20 weeks to rule out any gross malformation
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Nt was borderline raised Nipt n aminocentesis help rule out mental abnormalities not structural Eg noonans syndrome U need to undergo further testing Level two ultrasound at 18 weeks Fetal echo at 22 weeks
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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.