At my 20wk ultrasound I was 19wks and the doctor found two soft markers an echogenic intracardiac focus and a choroid plexus cyst. They did a blood test on me during my first trimester and at the beginning of my second trimester and I tested negative for everything (Down syndrome, Trisomy etc.). These soft markers can appear in normal pregnancies, but my doctors haven’t really mentioned anything to me even though I read these soft markers increase my babies risk for Down syndrome and Trisomy 18. Maybe I’m worried for no reason since my blood tests were negative and both soft markers have been known to dissolve in healthy babies by 24wks.... But, I’m just wondering if anyone has had this happen to them? I read a bunch of posts where people tested positive for Trisomy 18 and 21 but none in my situation. Any advice would be greatly appreciated. And of course at my next appointment I will bring it up since no one has talked to me about it yet.