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Can you test positive for 2 mutations of cystic fibrosis on one copy of a gene? I am 43 and have 2 mutations and they are testing my mother.
A friend just had the Cystic Fibrosis gene mutation blood panel done for 23 most common plus 9 rare mutations of CF, 32 total, all negative. Does this mean he is CF free and can safely have a child? I'm curious as to what these results actually mean?
What are the chances of passing on the Cystic Fibrosis gene if only one parent is a CARRIER? Other parent not a carrier.
Cystic fibrosis is a disorder of genes but which ones?
I have a cystic fibrosis mutation that showed no symptoms for 15 years, or since birth. Is it possible for symptoms to develop now or in the future?
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