Hi all,
We're having tests at the moment after our 12 week scan showed a nuchal translucency of 4.6mm. My blood work was also very odd, being extremely low in both HCG and PAPP-A. Other markers for chromosome issues are not present at this stage.
We are considering all our options and working on getting more information, but I wanted to ask about the long term outcome for children who were high risk pregnancies of this sort but were shown to be chromosomally normal with no structural defects? It seems to be such a new science that there is very little information out there. Can anyone share their experiences? Have there been developmental delays or issues that have cropped up after delivery? Just trying to arm myself with some information to help us through this process.
I have a separate thread going on antenatal testing about the tests themselves where some mumsnetters have kindly shared their stories, but thought this might be a more appropriate place to ask this question.
Thanks in advance
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Long term outcome for children with high nuchal measurement
6 replies
GaryWilmotsWedding · 29/06/2015 14:31
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