Hello, at my 12 week scan the baby had a nuchal measurement of 3.9 ('normal' is up to 2.9) and there was no nasal bone. Both of these indicated the possibility of chromosomal abnormalities. I had a CVS yesterday at the Fetal Medicine Centre and thank goodness they were able to tell me my results today. Everything came back clear. This is great news and I know I should be really pleased, but instead I'm thinking 'WHY hasn't the baby got a nasal bone?' and 'WHY was the nuchal fluid measurement so high?' I know the latter can sometimes mean there are heart problems and I'll need more scans to check that out, but does anyone know what else (if anything) might be wrong?