Event - Possible genetic testing

Pregnancy follow-up

Possible genetic testing

This testing, typically available for consideration between the 10th and 22nd weeks of pregnancy, offers insights into the genetic health of your baby, helping to identify any potential genetic disorders or conditions early on.

Be prepared for your possible testing

Top Asked Questions

What genetic tests are available at 11 weeks?

At 11 weeks, you can opt for Non-Invasive Prenatal Testing (NIPT), which screens for certain chromosomal abnormalities like Down syndrome, Edwards syndrome, and Patau syndrome using a sample of your blood.

How does NIPT work?

NIPT analyzes small fragments of fetal DNA that are circulating in the mother's blood to assess the risk of chromosomal abnormalities.

Is NIPT accurate?

NIPT is highly accurate in detecting certain conditions, but it's a screening test, not a diagnostic test. A high-risk result may require further testing, such as amniocentesis or chorionic villus sampling (CVS), for confirmation.

Should everyone get NIPT?

NIPT is recommended for those considered at high risk for chromosomal abnormalities, including women over 35, those with a family history of genetic disorders, or abnormal findings on an ultrasound. However, it's available to anyone who wants additional screening.

What other tests might be recommended around this time?

In addition to NIPT, you might also have the option for a nuchal translucency (NT) scan, which is an ultrasound performed between 11 and 14 weeks to measure the clear (translucent) space in the tissue at the back of the baby's neck, contributing to assessing the risk of chromosomal abnormalities.