Terrified - Omphalocele and/or Partial Molar Pregnancy experience??

Maltabet

Hi Ladies, I'm new here. I was already high risk because I'm epileptic. The MFM discovered a small omphalocele during our NT scan at 12w6d. I am going back for a follow up u/s this Friday and to meet with the genetic counselor. I kept asking the dr what this could all mean and she just kept saying she was concerned. (There is also a small concern of partial molar pregnancy, but I'm only equipped to deal with one thing at a time - and it seemed they were more concerned about the omphalocele)

We conceived during our third IVF (and had done Preimplantation Genetic Diagnosis) and I'm a wreck thinking I could lose my miracle baby. Anyone have any hope they can add?

Baby measured perfectly at 13w1d, heartbeat was 161, liver, heart, brain, kidneys (everything but a tiny bit of intestine) was where it should be.

According to the NT scan, our chance of DS is 1/5800 and chances of trisomony 13 or 18 is less than 1/10000

I assume if the intestines havent retracted back in by Friday, which seems unlikely according to the dr, I assume the next step is amnio Any other info?

How long does it take to get amnio results?

Thanks. Hope everyone else is doing well