Pre-natal screening helps identify potential genetic, chromosomal, and developmental conditions at an early stage, allowing timely medical guidance, informed decisions, and improved pregnancy management for both mother and baby.
Safe & Non-Invasive Tests
Most screening procedures involve simple blood tests and ultrasound scans that are completely safe, painless, and pose no risk to the mother or the unborn child during pregnancy.
Expert Medical Supervision
All diagnostic screenings are conducted under the guidance of experienced gynecologists, radiologists, and lab specialists, ensuring accurate reporting, professional interpretation, and proper follow-up support whenever needed.
Treatment Specialties
NT Scan (Nuchal Translucency Test)
Performed in the first trimester, this ultrasound measures fluid at the back of the fetus’s neck to assess the risk of chromosomal abnormalities and certain congenital conditions early in pregnancy.
Double Marker Test
A maternal blood test conducted during early pregnancy to evaluate the possibility of chromosomal disorders, helping doctors determine whether further diagnostic testing or monitoring is necessary.
Anomaly Scan
A detailed mid-pregnancy ultrasound that checks fetal organs, spine, limbs, and overall growth to detect structural abnormalities and ensure healthy development inside the womb.
Growth Monitoring Scans
Regular ultrasound scans track the baby’s growth, amniotic fluid levels, and placenta health, ensuring that development is on schedule and identifying any concerns that may require medical attention.
High-Risk Pregnancy Screening
Specialized diagnostic monitoring for mothers with medical conditions or pregnancy complications, offering continuous evaluation and preventive care to reduce risks for both mother and baby.
Genetic Counseling Support
Professional consultation to interpret screening results, explain potential risks, and guide families on next steps, ensuring clarity, reassurance, and well-informed pregnancy care decisions.
