Yesterday at my OB appointment they said that they saw some bright spots on the bowels during the ultrasound. (When I was in the hospital for neuro problems a few weeks ago they also mentioned that.) The doctor said that this can be an indicator of a chromosomal abnormality. There is also some gender ambiguity. (We had an elective ultrasound where they said it was a girl, but that her parts were just swollen.) I had the testing for downs/spinabifida earlier in my pregnancy and that came back fine. Has anyone had experience with this? They are trying to get me in with Children's & Women's hospital here ASAP but between this and my neuro problems, I'm at my wits end. I've done nothing but cry because all I want is for my baby to be ok. I can deal with problems with me, but not my baby. Oh, they also said that I have a hernia that may need to be repaired after birth, that is causing a bulge above my belly button. Sorry if this is all hard to understand, but I'm upset and could use some advice. Thanks.
Re: Chromosome abnormality.
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Remember they are soft markers indicators. We did further genetic testing which made us not worry as much too. We passed on the amnio when the doc said our chances were 1 in 100,000.
Try to relax and keep us updated on any further testing you have.
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So sorry you have to worry about this. I'm assuming by blood work you had the NT (which is just a screening, it's not diagnostic either way) or did you have testing like Materniti21/Panorama, etc.? If you didn't have the latter, maybe ask your doctor about having this test - just a blood draw but they isolate the fetal DNA from your blood and are accurate in detecting most common chromosomal abnormalities including sex chromosomal disorders. It's just a blood-draw and non-invasive like amnio. Because you had a soft marker, your insurance would likely pay for it (but check to be sure). Results back in about 10 days.
My friend had echogenic (white spots) bowel and heart that didn't show-up earlier, but showed-up on AS. Her doctor freaked her out and told her it was most likely T13 or 18 and started talking about next steps - amnio then termination before she missed her state's cut-off. She declined, her daughter was born perfectly healthy and turned 3 in June. Most of the time this does turn out to be nothing, your doctor has to inform you, refer you for further investigation. It's terrible that these things will stress anyone out and it's impossible not to worry, but most times everything is OK. Hugs to you.
I also had a soft marker with my first pregnancy, an echogenic intracardiac focus in the heart. I had a fetal echo and it was normal. My baby was born with no chromosomal issues. He's a smart, funny normally developing 2 year old.
As far as soft markers go, echogenic bowel is a pretty weak one. I doubt they'll recommend amnio unless it's for your peace of mind.