Advanced Prenatal Screening
We offer a range of specialized screening tests during pregnancy to provide valuable information about your baby’s health. These tests help in the early assessment of certain chromosomal abnormalities, offering peace of mind to expectant parents.
Informed Decisions
Our screening tests provide crucial information to help you and your doctor make the best decisions for your pregnancy journey.
High Accuracy
We utilize the latest technologies, including advanced NIPT, to ensure the highest possible accuracy in our screening results.
Expert Guidance
Our experienced team is here to guide you, explain the tests clearly, and help you understand your reports.
Our Prenatal Screening Tests
Double Marker Test
A first-trimester screening test (performed between 11-14 weeks) that measures two specific substances in the mother’s blood. It is combined with an NT scan to assess the risk for Down syndrome and other conditions.
Triple Marker Test
A second-trimester screening (15-20 weeks) that measures three markers in the mother’s blood 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, providing a higher detection rate for screening chromosomal abnormalities compared to the Triple Marker test.
NIPT (Non-Invasive Prenatal Testing)
A highly advanced blood test that analyzes fetal DNA from the mother’s blood. Performed from 10 weeks onwards, it offers the highest accuracy for screening common chromosomal conditions.