I wanted to share my experience with baby having been found to have an echogenic bowel at the 20 week / anomaly scan
The couple of days following this finding were quite scary for me so I scoured the internet looking for anyone whod gone through the same. What I found answered a lot of the questions I had so hopefully I will be able to add to that
Our 12 week / dating scan went smoothly and I had been feeling fine, with the exception of three almost back to back colds I'd had in the weeks leading up to it so I was optimistic when the time came for our 20 week scan
The grade 2 (bright as bone) echogenicity of the bowel was the only thing they found on screen that was of concern, and there were no other markers for abnormalities.
I was told four things could be the cause: Downs syndrome, cystic fibrosis, infection or just a very clear ultrasound. I was promptly taken for blood tests to screen for these; NIPT, CF gene carrier testing for both my DH and I and TORC.
It took weeks for all of the tests to come back but they've now all come back negative, to our immense relief.
I hope this helps anyone who might be going through the same situation. Sharing because I know how stressful it is and how much of your headspace it can take up so hopefully this will give you some hope.