Today my 12 week scan showed a nuchal of 3.3mm. While this is just below the 3.5mm where the NHS offers an amnio it is still thick. I await the combined test results.
This happened with DC2 who was 3.4mm. Wechose not to have further testing and she was born with no abnormalities.
Today I asked the doctor whether it could be that thick nuchals run in my family for no clinical reason. Dr said it sounded plausible but she had never seen studies on thick nuchal folds repeating themselves across children in the same family.
I wondered if anyone here has experience of more than one bad nuchal reading but healthy kids? I'd also live to hear of any other reassuring experiences.
TIA.