Prenatal screening provides a pregnant person with their own chance of having a child with:
- Down syndrome (also called trisomy 21)
Each pregnant person starts with a chance of having a child with a chromosome difference or change (chromosomes are explained under ‘Conditions Screened’) based on their age at the time of delivery. Screening adjusts this chance, either lowering or raising the chance based on the substances measured in the blood and/or measurements taken during the ultrasound.
No screening test screens for all chromosome abnormalities, so some may be missed. Screening also does not screen for every birth defect. Prenatal screening tests cannot tell you for sure whether or not your baby has one of these conditions, only the chance of it happening. To find out for sure if your baby has one of these conditions, you would have to consider a diagnostic test like chorionic villus sampling (CVS) or amniocentesis.
Screening tests can be done starting at 11 weeks of pregnancy and are available for ALL pregnant persons. Prenatal screening tests are optional – it is your choice whether to have a prenatal screening test. (Is Prenatal Screening Right for Me?)