The NIPT Test is a safe and highly accurate blood test that screens for common chromosomal conditions in a developing baby, such as Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18), and Patau syndrome (Trisomy 13).
Because the test only requires a simple blood sample from the mother, there is no risk to the baby. It can be done as early as 10 weeks of pregnancy, making it one of the earliest and most reliable screening options available.
NIPT helps expectant parents gain peace of mind and make informed decisions about their pregnancy with the guidance of their healthcare provider.
