I find this very interesting.  Not so much that you can be diagnosed at virtually any age for LOCAH, but moreover Natalie being diagnosed with it and ALL three of her children have it.

I was just assuming that Locah follows the same risk of passing a disorder on to your children as does SWCAH or CAH.  To be full blown SWCAH, both parents must have the gene and pass it on to the child(ren).  Does your husband have LOCAH also?

I’m sooo curious especially because I am researching some information on symptomatic carriers of CAH diagnosed later in life.  They do not have full blown CAH but are just carriers of the gene yet they have break through symptoms akin to CAH itself.

How does this work with your family?