Well the harmony doesn’t give a positive or negatives but the low risk result would be 0.0001% chance result. The high risk result is 99%
We had a 38% likelihood for Triple X syndrome (extra X chromosome). Not awful odds but terrible when compared with 1 in 10,000.
The calculation was based on the fact that they detected XXX cells in the sample but could not tell if they were from me, the placenta or the fetus.
We had to wait til my DD was born to have her chord blood tested. We didn’t want to do the amnio as the syndrome can be very mild so it wasn’t worth the risk of amnio.
Chord Blood test came back clear but the pediatrician said that blood testing wasn’t conclusive and wanted more bloods / tests run but to be honest by that stage I loved her and couldn’t take the stress of any more tests and we agreed we’d just review if she had any developmental delays (which she hasn’t)
Overall was delighted to have harmony as was 40 and worried about the 3 main syndromes (Downs, Petau and Edwards) so it did put my mind at rest for those concerns but would recommend avoiding the stress of the uncertainty sex anapleuoidy tests. I believe you can just ask for them not to test for that. Although you may not be able to find out the sex in that case.
Personally I don’t think the test is developed enough for the sex anapleuoidies and should not have been approved for those syndromes. The syndromes I refer to are triple x, turners syndrome and kleinfelter syndrome.