Carrier Testing

Carrier testing is a medical test that determines if a person carries a gene mutation linked to certain inherited conditions, without showing symptoms themselves. This is particularly important for recessive disorders, where a child must inherit the mutation from both parents to be affected. By identifying carriers, individuals and couples can assess the risk of passing genetic conditions to their children. Carrier testing is often recommended for specific populations or families with a history of genetic disorders, providing valuable information for family planning and healthcare decisions.