“Amniotic Fluid Karyotype Test – Prenatal Chromosomal Analysis for Genetic Disorders” has been added to your cart.
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AED2,150.00
Chromosomal Studies – Amniotic Fluid Karyotype is a prenatal diagnostic test that analyzes fetal chromosomes using a sample of amniotic fluid. It detects chromosomal abnormalities such as Down syndrome, trisomy 18, and structural rearrangements.
Sample Type : Amiotic Fluid
Methodology : Conventional Cytogenetics: Culture + Chromosome analysis
TAT : 30 Days
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AED650.00
The Anomaly Scan is a detailed ultrasound performed between 18-22 weeks of pregnancy to assess fetal development and detect structural abnormalities. It examines the baby’s organs, brain, spine, heart, limbs, and placenta, ensuring proper growth and identifying potential concerns early.
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AED3,950.00
Beta Thalassemia by PCR is a molecular diagnostic test designed to detect mutations in the HBB gene responsible for beta thalassemia.
Sample Type : EDTA Whole Blood
Methodology : PCR
TAT : 4 Weeks