Hi all,
I posted couple days ago here that an administrative error occurred during our 12week scan, which ultimately led to Chorionic Villus Sample test being carried out.
Initially they suggested that there was a 1 in 2 chance of down syndrome, and after the error was identified, risk went down to 1 in 5000, and in 1 in 20,000 for other anomalies.
It's worth highlight the fetal anatomy checks all came back normal. Nuchal Translucency was 1.6mm so within normal ranges.
Doctors were very apologetic about the error, but we were still considering complaining as initially we felt an invasive procedure that increased risk of miscarriage was done for no reason.
Yesterday the doctor called again advising trisomy 13 had been found in the placental DNA. She stressed the scans looked completely normal, so it's possible that this is just the placenta. I've done extensive research, and while this is possible - it's quite rare. So now it appears we have a baby that scanned as normal, who mistakenly had a CVS and has tested positive for 1 in 20000 anomaly.
Needless to say partner and I are distraught and devastated. Not sure what I'm hoping to get, perhaps insight or advice from anyone who may have been in a similar position or heard of a similar case.