Even though the ped. endo has decided our little foster baby does not have CAH, I have been reading the message board.  The endo has decided he won’t do the NCCAH testing nor DNA testing and has just told us to watch for signs of early puberty and advanced bone age (though no testing on that was done or is planned so I don’t know how we watch for that).  However, I have been seeing mention of 21 hydroxylase and other types of problems.  I was wondering if there is more testing that should have been done before saying he doesn’t have CAH.  He had the initial screening as a newborn that came back positive for CAH.  After that, the endo came into the picture and did a 17ohp and a renin test.  (We then did weekly sodium and potassium testing).  He ordered one more renin test (which had come down a lot) and then only followed with 17ohp testing from then on until he said he does not have CAH.  Is there other testing that should have been done for some of these other deficiencies?