Hi everyone! Last week, I had my NL scan which, combined with the blood work, resulted in a 1:26 risk of our baby having DS (and 1:88 risk of trisomy 13/18). Naturally, we're scared, since we weren't expecting those numbers at all. I'm in my mid-twenties.
The NF was 2,90 which was a bit on the thicker side according to the midwife, and my bloodwork was a bit weird, we didn't get a lot of information on that. After googling frenetically, I found out that the beta-hcg level should be around 1 MoM, which it was - 1,20-something, if I'm not mistaken - but the papp-a levels were really low, like 0.223 or something.
I'm also a carrier of a balanced translocation. It shouldn't affect chromosome 21 (my BT is 5;6) but does anyone know if that could mess up the results, giving a false positive? If it's the bloodwork that is the problem, won't NIPT show the same issue and risk a false positive again?
Sorry for all these questions. I'm terrified of losing this baby since we suffered a loss in August, our first pregnancy, at 18 weeks due to our CVS. 