The Genetics of Cystic Fibrosis
Cystic fibrosis (CF) is a genetic disease. This means that CF is inherited. A child will be born with CF only if two CF genes are inherited--one from the mother and one from the father. A person who has only one CF gene is healthy and said to be a carrier of the disease. A carrier has an increased chance of having a child with CF.
Once parents have had a child with CF, they have a one in four, or 25 percent chance, that each additional child will be born with CF. This means that there is a three out of four, or 75 percent chance, that additional children will not have CF. However, these children may be carriers of the CF gene.
Because most often a family has no history of CF, the diagnosis comes as a surprise to parents. Since both parents are healthy, they had no prior knowledge that they carried the gene, or that they passed the gene to the pregnancy at the same time.
Genes are found on structures in the cells of the body called chromosomes. Each cell normally contains 46 total, or 23 pairs of chromosomes. The seventh pair of chromosomes contains a gene called the cystic fibrosis transmembrane regulator (CFTR) gene. Mutations or errors in this gene are what cause CF. This gene is quite large and complex. More than 1,800 different mutations in this gene have been found that cause CF.
According to the Cystic Fibrosis Foundation, the risk for having a mutation in the gene for CF depends on your ethnic background if you have no family history of CF:
Risk of CF Mutation
Risk of Child with CF
1 in 29
1 in 2,500-3,500
1 in 46
1 in 4,000-10,000
1 in 65
1 in 15,000-20,000
1 in 90
1 in 100,000
A sweat chloride test to measure the amount of salt in your sweat is usually the first test done to try to diagnose CF.
Testing for the CF gene can be done from a small blood sample or from a cheek swab, which is a brush rubbed against the inside of your cheek to obtain cells for testing. Laboratories generally test for the 20 or so most common mutations.
Many people with CF have mutations that have not been identified. In other words, all of the genetic errors that cause the disease have not been discovered. Because not all mutations are detectable, a person can still be a CF carrier even if no mutations were found by carrier testing.
Testing for the CF gene is recommended for anyone who has a family member with the disease, or whose partner is a known carrier of CF or affected with CF.