The CF specialist called today and said he is 95% sure that my daughter doesn't have cf. He said she does have a very rare mutation and the other gene has a polymorphysm(not sure on spelling).
She has to do one more test so we know for sure and its the NPD test. They are suppose to call and schedule us sometime next week.
Thank you to everyone who responded to my posts and for all your advice!!
Any thoughts?
She has to do one more test so we know for sure and its the NPD test. They are suppose to call and schedule us sometime next week.
Thank you to everyone who responded to my posts and for all your advice!!
Any thoughts?