My 20 week scan showed an echogenic bowel. This was an isolated finding as there were no other soft markers or any other problems. The finding was confirmed 5 days later by a consultant who redid the scan. He did an amnio straight away to test for downs, edward and patau's syndromes, CMV and toxoplasmosis. They took blood tests to check if me and my husband are carriers for cystic fibrosis.
We are waiting for the results now which will take over two weeks because of the bank holiday and I have been looking on the internet for any statistics but unfortunately I can't find any consistency so I don't know what to believe. Has anyone had a similar experience and managed to get any advice on what the likelihood is of any of the above tests coming out positive?
Unfortunately all the doctor would say was that the likelihood of one of the tests being positive was 'unlikely' - to me that could mean anything under 50% and I don't find these odds particularly reassuring. I had a 1 in 100,000 result in my downs syndrome screening at 11 weeks which had really put my mind at rest until this happened.
It seems like such a long time to wait for the results - has anyone ever phoned up early for their results and got them?
Any advice would be much appreciated.
Thanks