Hi all, first time posting. I am 16+2 with my first baby after over a year of trying. At 12 weeks found out baby had micrognathia (small chin) but everything else looking normal. I was advised to have CVS which I did and all came back clear. Just been for another scan today and met with the consultant who still has concerns. They have mentioned treacher Collins syndrome which myself and my husband thought would have been ruled out on CVS / genetic test.
now awaiting a referral to a geneticist to see if they’ll do any further investigations. I feel left in the lurch a bit with whirling thoughts! Anyone had similar and can share their journey or experiences? Thank you x