My first daughter has 21-H salt-wasting CAH. She is 2 and has already had surgery. I have a 6 1/2 week old daughter who was tested immediately at birth, state tested at 48 hours old, at 2 weeks, and this past Wed. at 6 weeks. The first test for 17 OHP came back 704, the state test was negative, and the 3rd test was 406. We are waiting the results of the last test. My question is; since my 1st daughter is 21-H saltwasting, is that what we produce genetically or can you have any variation of CAH, even late onset in your children? My 2nd daughter is doing fantastic. She is gaining weight and thriving. Quite a difference from my 1st daughter. She has no ambiguity but the doctors aren't sure if that could be a result of my taking dexamethasone for 3 weeks in the beginning of my pregnancy. The endo said the reason for the levels could be a natural progression of what she received from me. He said that he thought if newborns were tested like my daughter was that there would be some that would show the same results. Has anyone else experienced this? Thank you for your input.