Hi, I am 15 weeks pregnant. A couple of weeks ago, I had my genetic blood draw to test for abnormalities, trismonies, etc. My OB contacted me yesterday to know that the blood detected a XXY chromosome that could indicate my sweet boy. Has Klinefelters Syndrome. Of course, I instantly googled this syndrome and it scared me... it seems, he should be able to lead a completely ordinary life. I will be sent to a high risk doctor for further testing, but will opt out of the amino, due to its side effects. Does anyone know anything about this syndrome? Am I setting my child up for failure? I’m putting myself into a panic. :(