Hi Ladies,
I posted this on the high risk board too, but thought I would see if anyone else over here had any experience with this.....
I had a routine baseline cervical length u/s this morning and Dr. said baby B had a small spot on the heart that is basically a small calcified part (aka "bright spot" or in fancy medical terms an "echogenic intracardiac foci") in the heart muscle. He mentioned that it could be a "soft" marker for down syndrome, but since my 12 week NT scan & bloodwork revealed a < 1:3600 chance of either baby having down syndrome, my odds were very low. But now, b/c they found this marker it would increase the odds to 1:1800. From the research I have read it basically sounds like if you are NOT at high risk of having a baby with down syndrome (i.e. < 35 y/o, low bloodwork levels, good NT results, & no other u/s abnormalities) it is not associated with an increased risk.
I feel like the Dr. gave me the information he "had" to, but I feel like it is making me worry for no other reason than a "possibility", if even that.
Any info would be greatly appreciated, TIA!!!
Re: XP: Echogenic Intracardiac Foci ???
Cardiac foci are seen in about 1% of all pregnancies. I know some MFMs who have stopped reporting them all together if there are no other markers for genetic anomalies.
HTH.
DD had two soft markers--chloroid plexus cyst and single umbilical artery--and none of the dr's were nearly as worried as we were. Both my OB and MFM said that if they weren't required to tell me, they would prefer not to b/c those things turn out to be innocent so much of the time. Of course, I worried right up until DD was delivered and I saw her, but I'm also a worrier by nature.
My oldest DD had two markers also, she had the bright spot in her heart and a choroid plexus cyst. Scared us to death, but the doctors never really seemed all that worried. I worried myself sick about it the rest of my pregnancy and she came out perfectly healthy!
My best advice is to not google it, I did, and it made me worry so much more.