Carrier Screening

Carrier screening is a genetic test that helps individuals and couples understand their risk of passing on genetic disorders to their children. During prenatal or preconception counseling, this test checks if one or both partners carry specific genetic mutations linked to conditions like cystic fibrosis or sickle cell anemia. If one partner is a carrier, the other may be tested to assess the likelihood of having an affected child. This information empowers families to make informed choices about family planning and health management, ensuring they understand potential risks and available options.