JRaeCollins
New member
I am new to this site and am looking for some info regarding my sons diagnosis. He is six weeks old and has two mutations for CF but I don't really understand how the two work together. He has one heterozygous Delta F508 mutation which I believe is a common one. The other mutation is (TG)11-5T variant. Can anyone help explain to me what I am dealing with? From what I have been reading, he may not have the full symptoms of CF. He may be infertile due to the CBAVD, or he may have little or no symptoms of CF and simply be a carrier. We are still waiting to confirm the blood tests so in the meantime, any help in understanding these two mutations would greatly be appreciated.
Thanks,
Jessica
Mother to Cody 2 1/2 years, no known CF
Mother to Cage, 6 weeks, diagnosed with two mutations
Thanks,
Jessica
Mother to Cody 2 1/2 years, no known CF
Mother to Cage, 6 weeks, diagnosed with two mutations