We were given a 1 in 10 chance for one of the trisomies at combined screening (and 1 in 100 for another), mostly because of a thick nuchal translucency.
Our chorionic villus sampling and fetal echo scans have all been good, and same for anomaly scan. Now not long to go - having regular growth scans which look normal although femurs on 25th percentile? I know shorter legs can be a soft marker but I think that's usually below 5th percentile or in comparison with high head or abdominal circumference (our's is around 50th for both.)
Was overjoyed at results initially but still worry as I know that CVS false negative results are rare but do happen. We'll love our baby whatever but I keep thinking it's too good to be true.
Has anyone been in same position and all was fine? Thanks