Carrier Screening Is A Genetic Test
Carrier screening is a genetic test used to identify individuals who carry one copy of a gene mutation that, when present in two copies (one from each parent), causes a genetic disorder. This screening is an essential tool in reproductive genetics and plays a vital role in helping individuals and couples understand the risks of passing on inherited genetic conditions to their children. As genetic understanding has advanced, carrier screening has evolved into a more widespread and sophisticated practice that can provide critical information for family planning and reproductive decision-making.
