Does anyone have any experience of the above? This is my first pregnancy not to end in miscarriage. It's an IVF pregnancy with a euploid embryo.
At 20 weeks, it was identified that the baby had a centrally placed heart (rather than left) as well as I had a single umbilical artery. We were referred to fetal medicine and then to a cardiac twice and all these scans couldn't find anything structurally wrong with the baby or heart and concluded it was likely 'benign variation.' They did mention genetic disorders could be a possibility but given the embryo was tested they advised that an amnio probably wasn't worth the risk.
At a 32 week growrh scan yday, we got told we had moderate polyhydramnios and that the baby's stomach was measuring a bit small, although still within normal parameters. They said the baby's stomach does have some amniotic fluid in so it is swallowing (which is good) but that it wasn't 'really full.' Our notes also referenced PRUV (Persistent right umbilical vein) which wasnt discussed and I don't really understand but it appears to be quite rare.
Does anyone have any experience of the above and how did it work out for you? I am panicking that all these separate things can't be a good sign and maybe there is something seriously wrong with my baby. I know all I can do is wait and see really but would love to hear from anyone else who has experienced similar.