We've just had our NT scan at 12+4.
DS risk is 1 in 10000 (trisomy 18 and 13 risk less than 1 in 20000).. Has any one had a child with DS / chromosomal abnormalities with a risk this low ? I'm aware that it is a screen so of course there can be false negatives and positives. They did not mention if the nasal bone was not present however.
Many thanks