Invasive Prenatal Testing

Invasive prenatal testing involves procedures where a small sample of a pregnant person’s blood, amniotic fluid, or placental tissue is collected to assess the health of the developing baby. These tests can detect genetic conditions, chromosomal abnormalities (like Down syndrome), and other potential issues. Common methods include amniocentesis and chorionic villus sampling (CVS). While these tests provide detailed information, they carry small risks, such as miscarriage. They are typically recommended when there is a higher chance of genetic concerns based on screening results or family history.