Assess the risk of chromosomal abnormalities
Down’s syndrome screening is a prenatal assessment designed to evaluate the likelihood of the baby having chromosomal conditions, particularly Down syndrome (Trisomy 21). It involves a combination of maternal blood tests and specialized ultrasound markers, such as the nuchal translucency measurement, performed during the first and second trimesters of pregnancy. These tests do not provide a definitive diagnosis but help identify the level of risk, allowing for further diagnostic testing if required. Early screening enables timely decision-making, appropriate medical guidance, and better pregnancy management.
First & Second Trimester Tests
Risk Calculation
Genetic Counseling
Combined Screening Approach
Early Risk Detection
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Consultant Obstetrician & Gynecologist
This is recommended for pregnant women who need early screening for chromosomal conditions.
Women above 35 years
High NT measurement
Family history
Screening performed during the first trimester for early detection.
Includes ultrasound (like NT scan) and blood tests for better accuracy
Clear explanation of results and next steps.
Helps identify the possibility of Down’s syndrome early.
Screening involves simple and safe procedures.
Allows timely decisions and further testing if needed.
Our centers are equipped with advanced diagnostic laboratories, fetal monitoring systems, and 24/7 emergency care facilities to ensure comprehensive women’s healthcare.
Madinaguda
Nallagandla
Zaheerabad
Isnapur
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Find answers to common questions about our women care services and treatments.
No, it only shows risk. Further tests may be needed for confirmation.
Doctors will recommend further diagnostic tests and guide you.
