Advanced Prenatal Screening Tests
We offer a range of specialized blood tests to screen for chromosomal abnormalities during pregnancy. These tests help provide valuable information for you and your doctor to ensure the best possible care.
Double Marker Test
A first-trimester screening test (11-14 weeks) that measures two pregnancy-specific substances in the mother’s blood. It’s combined with an NT scan to assess the risk for Down syndrome and other chromosomal conditions.
Triple Marker Test
A second-trimester screening test (15-20 weeks) that measures three markers in the mother’s blood (AFP, hCG, and Estriol) to assess the risk for Down syndrome, Trisomy 18, and neural tube defects.
Quadruple Marker Test
An enhanced second-trimester test that measures four markers, including Inhibin A. This addition provides a higher detection rate and greater accuracy for screening for chromosomal abnormalities compared to the Triple Marker test.
NIPT (Non-Invasive Prenatal Testing)
A highly advanced and accurate blood test that analyzes fetal DNA circulating in the mother’s bloodstream. NIPT can be performed from 10 weeks onwards and screens for common chromosomal conditions with a much higher accuracy than marker tests.