Had our genetics consult yesterday. First off... Everything is fine... No follow up needed. He explained that two soft markers, specifically Echogenic foci were seen in the heart. They are areas of increased calcification. A better predictive test of chromosomal abnormalities would be an IPS... My blood work... Which was fine. Basically, technology is showing the more.... And therefore more follow-up is needed. They are trying to change the criteria to higher number of markers before a genetics consult. He was lovely, did a subjective assessment, measured my belly and listened to baby. Told us the markers have no short or long term tern effects... Everything is as it should be.
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