I'm wondering if anyone else has had a mildly echogenic bowel on their 20 wk morph scan?. My NT scan was perfect with very low odds for down syndrome and trisomy. The rest of my 20wk morph was perfect, which has left me totally stumped. I had bloods taken today to rule out cystic fibrosis and a raft of other viruses/illnesses. The hardest part is waiting 2 weeks for the results to come back. I'm interested to hear if anyone else has experienced the same problem and what the outcome was.