<span><span class="post-color-blue">Me:30 DF:29</span><br></span>
<span><span class="post-color-blue">DS1:Dec 13</span><br></span>
<span class="post-color-blue">DS2:May 2020</span>
Me: 30 | H: 30
MMC: 6/2017 (10w5d)DS: May 2018TTC #2
BFP: 9/1/19 EDD: 5/14/20
I had my anatomy scan today and all looked well except they found a couple soft markers for trisomy 18/21. There were 3 echogenic foci in the left ventricle of his heart and a choroid plexus cyst in his brain. Apparently these are most likely normal findings but the fact that they aren’t isolated because there are two of them may be more worrisome. The next step would be NIPT testing, which we already had done and came back negative. So that’s positive. The stats lean towards this not being an issue but I can’t help but be nervous about it. The OB said if we are really nervous we could see a genetic counselor and have an amniocentesis. I don’t think we will go that far, right now we have a growth scan scheduled in 8 weeks. Feels so far away. Has anyone had similar findings on their anatomy scan?