I had my 19w anatomy scan on Monday and the radiologist informed me that baby girl has multiple choroid plexus cysts, which I've been told can be totally normal for 1-2% of pregnancies. Then I received a call yesterday from the genetics counselor to tell me that the baby also may have a bright spot on the bowel, but they are unsure if it was the lower grade US itself or truly a marker. They scheduled me for a level 2 scan with a perinatologist next Monday (thank goodness I don't have to wait very long).
I know that I shouldn't worry before I know for sure, and the second marker is still an unknown... but I can't help it! My mind is completely clouded by this, and I can't stop researching it just to be assured that everything could be just fine. The next 5 days are going to be a bit stressful.
Anyone else have these markers? If so, how did it turn out for you?
Thanks for any input.
Re: Soft markers for T18 and T21
I appreciate the encouragement and shared experience.
With my daughter they were still present at 35 weeks and with my son they were gone by the time we got to the level 2 ultrasound 4 weeks later. All that to say that if they go away or stay is really not the important part - it's about everything else they see on the level 2 ultrasound. If everything else looks good it really is nothing to worry about.
Did you do the Nucal translucency? If so that also can be reassuring. You can ask about doing the harmony test becaue you may qualify for that now, might be worth at least asking.
Married to DH 10.29.11
DD born 1.26.13
DS born 6.12.14
#3 due 12.6.16