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. This type of inheritance is called autosomal recessive. Autosomal means that the gene is on one of the first 22 pairs of chromosomes which do not determine gender, so that the disease equally affects males and females. Recessive means that two copies of the gene, one inherited from each parent, are necessary to have the condition. Once parents have had a child with CF, they have a one in four, or 25 percent, chance with each subsequent pregnancy for another child to be born with CF. This means that there is a three out of four, or 75 percent chance, for another child to not have CF.
The birth of a child with CF is often a total surprise to a family, since most of the time there is no previous family history of CF. Many autosomal recessive conditions occur this way. Since both parents are healthy, they had no prior knowledge that they carried the gene, nor that they passed the gene to the pregnancy at the same time.
Genes are founds on structures in the cells of our body called chromosomes. Each cell of the body normally has 46 total, or 23 pairs of chromosomes. The seventh pair of chromosomes contains a gene called the CFTR (cystic fibrosis transmembrane regulator) gene. Mutations or errors in this gene are what cause CF. This gene is quite large and complex. Over 1,000 different mutations in this gene have been found which cause CF.
The risk for having a mutation in the gene for CF depends on your ethnic background (for persons without a family history of CF):
|Ethnic Background||Risk of CF Mutation||Risk of Child with CF|
|Caucasian||1 in 29||1 in 2,500-3,500|
|Hispanic||1 in 46||1 in 4,000-10,000|
|African-American||1 in 65||1 in 15,000-20,000|
|Asian||1 in 90||1 in 31,000|
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 most common mutations. The diagnosis is confirmed by another test call the sweat chloride test.
There are many people with CF whose mutations 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.
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