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Hi all, I have just been diagnosed with LOCAH having had the synacthen stimulation test carried out a few weeks ago. It was picked up because I was diagnosed with PCOS and my husband is infertile and ultimately, we are to start ICSI treatment this year. I have now been referred to an endocrinologist for genetic karyotyping. I am keen to find out what are the risks to any future children of mine. Are they at risk of having LOCAH or even CAH? Any info or advice would be much appreciated.
