Fetal Genetic Testing

Fetal genetic testing involves analyzing a developing baby’s DNA to identify potential genetic conditions or chromosomal abnormalities. It can be done during pregnancy through procedures like amniocentesis or chorionic villus sampling (CVS), which collect small samples of amniotic fluid or placental tissue. These tests help expectant parents and healthcare providers understand if the fetus has genetic issues such as Down syndrome or other inherited conditions. While they provide valuable information, they also carry some risks and ethical considerations. Fetal genetic testing supports informed decision-making and early intervention planning for the health of the baby.