Because CF is an autosomal recessive genetic disorder, it can’t be prevented. But if a woman knows she has CF, she can take steps to lower the chance of passing the gene mutation to her child. For example, she can have a healthy baby through in vitro fertilization (IVF) if she has the mutation. She and her partner could also use donor sperm, but they should take steps to make sure that they both have the mutation (they can test for it at the same time). This way, their child would not inherit the mutation.
It’s also possible for a woman with CF to have a baby through donor eggs. She would need to have the mutation, but the donor egg would not be affected by CF. This way, neither parent would have the mutation. If a woman is not planning to have children, she may want to ask her doctor if she is a CF carrier.
CF is passed from parents to children through the CF gene. There is one version of the CF gene for each person. If someone has the CF gene mutation, that person has CF. Many of these people are told they have CF, but CF can be difficult to diagnose. That's why everyone needs to be screened for CF.
CF is a very serious condition that can significantly affect your child’s health, quality of life, school and social activities, and ability to grow and develop. It is caused by a single gene, and is passed down through the DNA of family members. The gene mutation does not show up in CF carrier testing.
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