prenatal genetics

Prenatal genetics involves studying a baby’s genes before birth to understand their health and development. It includes testing the DNA from the mother, the fetus, or the amniotic fluid to detect genetic conditions or disorders caused by changes in genes or chromosomes. These tests can help identify risks for conditions like Down syndrome or cystic fibrosis, allowing parents and doctors to prepare or make informed decisions. Prenatal genetic screening and diagnostic tests are valuable tools for ensuring the best possible health outcomes for the baby and family.