Cystic Fibrosis Gene Mutation Test

A Cystic Fibrosis Gene Mutation Test is a genetic test that identifies mutations in the CFTR gene, which can cause Cystic Fibrosis (CF). CF is a genetic disorder that affects the respiratory, digestive, and reproductive systems. This test helps in diagnosing CF and determining carrier status.

The test is recommended for individuals with a family history of CF, couples planning to have children, and those with symptoms like chronic lung infections, digestive issues, and infertility. It's essential for prospective parents to assess their risk of passing CF to their children.

The test is typically done using a blood sample or a cheek swab. The DNA from the sample is analyzed to detect mutations in the CFTR gene. Genetic counselors and healthcare providers can guide you through the process.

The cost can vary widely depending on your location and insurance coverage. Some laboratories offer affordable options, and insurance plans may cover part or all of the expenses. It's essential to check with your healthcare provider and insurer for specific pricing information.