Fetal Health

  • Growth Scan

    Growth Scan: Advanced Fetal Ultrasound for Precise Pregnancy Monitoring

    750,00 د.إ

    A Growth Scan is a specialized ultrasound designed to monitor your baby’s development during pregnancy, providing essential insights into their well-being. Typically performed in the third trimester, this detailed scan assesses fetal growth, amniotic fluid levels, placental function, and blood flow to ensure your baby is thriving.

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    Triple Test Prenatal Screening – Comprehensive Maternal & Fetal Health Check

    650,00 د.إ

    The Triple Test: Comprehensive Screening for Maternal and Fetal Health is a non-invasive prenatal blood test that evaluates three key biomarkers—AFP, hCG, and estriol—to assess the risk of fetal chromosomal abnormalities such as Down syndrome and neural tube defects.

    Sample Type : Serum

    Methodology : Enzyme-immunoassay

    TAT : 3 Days

  • Veritas NIPT Basic – Non-Invasive Prenatal Test for Early Genetic Screening

    Veritas NIPT Basic – Non-Invasive Prenatal Test for Early Genetic Screening

    1.050,00 د.إ

    Veritas NIPT Basic is a non-invasive prenatal test (NIPT) that screens for common chromosomal abnormalities, including trisomy 21 (Down syndrome), trisomy 18, and trisomy 13, using a simple maternal blood sample. It offers high accuracy, early detection from the 10th week of pregnancy, and a low false-positive rate, reducing the need for invasive procedures. The test is safe for both mother and baby, providing fast and reliable results to support informed pregnancy decisions.

    Sample Type : Maternal blood

    Methodology : NGS

    TAT : 10 Days

  • Veritas NIPT Extended

    Veritas NIPT Extended

    1.499,00 د.إ

    Veritas NIPT Extended is a non-invasive prenatal test that screens for a broad range of chromosomal abnormalities with high accuracy. It analyzes fetal DNA from a maternal blood sample as early as the 10th week of pregnancy, detecting common conditions like Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18), and Patau syndrome (Trisomy 13), as well as sex chromosome aneuploidies and select microdeletions.

    Sample Type : Maternal blood

    Methodology : NGS

    TAT : 10 Days

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