Cystic Fibrosis
Mode Of Inheritance
CF is a classical autosomal recessive disease, in which affected patients are born to parents who are both carriers—that is, they have a mutation in one of their two CF genes. Carrier couples have a one-in-four risk of producing an affected child with each pregnancy. The carriers themselves are completely asymptomatic and even have normal sweat chloride tests.
Additional topics
Medicine EncyclopediaGenetics in Medicine - Part 1Cystic Fibrosis - Clinical Features, Mode Of Inheritance, Treatment, The Cystic Fibrosis Gene And Cftr Protein, Cystic Fibrosis Dna Testing And Screening - Laboratory Diagnosis