Cystic Fibrosis (CF), a genetic condition, that occurs when the affected gene is inherited from both the mother and the father. In New Zealand about one in 25 people are carriers of CF.
The CFTR* gene gives instruction to our body’s cells to make a protein that controls the movement of salt in and out of the cells. If there is a coding error in the DNA of the gene it can reduce or eliminate its effectiveness. In CF, these changes in salt movement cause changes to the water balance in cells and cause mucus to become thickened and to build up, leading to the health complications associated with CF.
CFTR: Cystic Fibrosis Transmembrane Conductance Regulator
In New Zealand, among people of Caucasian descent the occurrence of a person having one copy of the CF gene is approximately 1 in 25. This is much lower in African, Asian and Polynesian populations.
People with one CF gene are called ‘carriers’ and generally have no symptoms of CF. Being a genetic carrier is not the same as being a carrier of a viral illness like the flu, which can be caught by others. CF is not contagious, the only way someone can have CF is through inheriting faulty CFTR genes from both their parents.
For more information on the genetics of Cystic Fibrosis please view this brochure
For diagrams showing the inheritance pattern of the CF gene please visit our page Genetic Inheritance of Cystic Fibrosis