Genetic Carrier Screening

Genetic carrier screening is a medical test that helps determine if an individual carries a gene for certain inherited conditions, even if they show no symptoms themselves. This is important for prospective parents, as it can reveal the risk of passing genetic disorders, like cystic fibrosis or sickle cell anemia, to their children. The screening involves a simple blood or saliva sample and analyzes specific genes. Knowing one's carrier status can guide family planning decisions and inform healthcare providers on potential future health issues for children. It’s a proactive approach to understanding genetic risks.