Our Fetal Medicine department is equipped with state-of-the-art technology and led by Dr. Jasmine Lall, who brings her extensive training and expertise to the centre. We offer a range of services to monitor and ensure the health and development of your baby throughout pregnancy.

• First Trimester Scan (NT Scan): Essential early pregnancy screening to detect potential chromosomal abnormalities.
• TIFFA Scan (Anomaly/Level II Scan): Comprehensive anomaly scan performed between 18-22 weeks to check for structural abnormalities.
• Advanced 3D/4D Sonography: Provides high-resolution images of the fetus, offering a detailed view of fetal structures.
• Genetic Sonogram: Specialized ultrasound to assess genetic conditions and abnormalities.
• Fetal Neurosonogram: Detailed imaging of the fetal brain to identify any neurological issues.
• Fetal Echocardiography & Arrhythmia Study: Detailed examination of the fetal heart to detect any congenital heart conditions.
• Fetal Growth and Doppler Study: Monitoring fetal growth and assessing blood flow to ensure the baby’s well-being.

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Our General Diagnostic Services provide a comprehensive range of scans and tests to support overall health and well-being.

• Early Pregnancy Scan (<11 weeks): Initial scan to confirm pregnancy and check for early developmental markers.
• First Trimester Screening (11-14 weeks): Combines ultrasound and biochemical screening to assess the risk of Down’s Syndrome.
• Early Anomaly Scan (16-18 weeks): Preliminary scan to detect any early structural anomalies.
• Detailed Anomaly Scan (18-22 weeks): In-depth scan to thoroughly check for any fetal anomalies.
• Second Trimester Fetal Echocardiography (16-24 weeks): Detailed scan of the fetal heart during the second trimester.
• Fetal Growth Surveillance: Regular monitoring to ensure the fetus is growing properly.
• Fetal and Maternal Doppler Studies: Assessing blood flow in the fetus and mother to monitor the health of both.
• Follicular Imaging in Assisted Reproduction: Ultrasound imaging to support fertility treatments.

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We offer a range of genetic and prenatal testing options to ensure comprehensive screening for potential genetic disorders.

Down Syndrome Screening:

• First Trimester Screening (11-14 weeks): Early detection using ultrasound and biochemical markers.
• Quadruple Test: A blood test in the second trimester to screen for Down’s Syndrome.
• Non-Invasive Prenatal Testing (NIPT): A highly accurate blood test to screen for chromosomal abnormalities.

Advanced Genetic Tests:

• Combined Test: Screening combining ultrasound and blood test results.
• NIPT: Non-invasive testing for chromosomal abnormalities.
• QF PCR: Quantitative Fluorescence Polymerase Chain Reaction for rapid genetic testing.
• Karyotyping: Analysis of chromosomes to detect genetic abnormalities.
• FISH: Fluorescence In Situ Hybridization for detailed genetic analysis.
• Microarray: Comprehensive genetic testing for a wide range of conditions.
• Mutation Study: Detailed analysis to identify specific genetic mutations.

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