Prenatal screening and testing
What is prenatal screening?
Prenatal screening won't tell you if your baby has a health condition, but it can assess your risk. Learn more here about deciding whether to have a p...
Pregnancy checkups, screenings and scans
Knowing what check-ups, screenings and scans to have and when to have them during your pregnancy is important information for every pregnant woman.
Genetic carrier screening
Screening for carrier status is a blood test to see if you carry genes that are linked to certain health conditions. Learn more about this test here.
Genetic counselling
Genetic counselling may be recommended for people who have a history of hereditary disorders. Find out if counselling can be helpful and what to expec...
Non-invasive prenatal testing (NIPT)
A non-invasive prenatal test (NIPT) is a sensitive test to screen for Down syndrome and some other chromosomal disorders early in pregnancy.
Screening for Down syndrome
Down syndrome is a chromosomal disorder that affects 1 in 1,00 babies. Find out about the screening and diagnostic tests that can detect the condition...
Nuchal translucency scan
A nuchal translucency scan is an ultrasound scan that helps in estimating your risk of having a baby with chromosomal abnormality. Learn how the test ...
Morphology scan
A morphology (or anomaly) scan will likely be offered to you at 18-20 weeks of your pregnancy. Learn about what it can tell you and how it is performe...
Chorionic villus sampling (CVS)
Chorionic villus sampling (CVS) is a test done during pregnancy to detect genetic abnormality in an unborn baby by sampling cells from the placenta.
Amniocentesis
Amniocentesis is a diagnostic test, done during pregnancy, to assess whether the baby has an abnormality or serious health condition. Find out what’s ...