Okay, I’m confused. I requested copies of the results to be sent to me. The endo nurse called said my son’s dna test normal (no mutation). So he is not a carrier, my daughter’s test shows one mutation on axon 7. So what does that mean? I thought she should have 2 mutations, and she did not stipulate what type of mutation it was. She had no idea what they meant.

 Okay my questions are, since I have locah shouldn’t my son have at least one mutation from me? and shouldn’t my daughter have two, since she has locah too???? I would really apreciate some insight, from some of you experienced friends out there.