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I got sent a report this morning from fetal medicine from my fast results from my amniocentesis.
My test was sent to Glasgow.
An apparently normal complement was detected for chromosomes 13 18 and 21. An XY sex chromosome complement was detected indicating the fetus is male.
This result supersedes the previous NIPT screening results.
My amniocentesis was done as i had a 60% chance from my harmony bloods of baby having Klinefelter XXY.
Does this definitely means this fast result on the amnio has ruled this out.
did they explain to you what the results for the fast result were for?
It looks like the baby is fine in terms of T13, T18 and T21 and XY suggests that it's ok and not XXY. I personally would phone them and ask if this rules out Klinefelter too.