Prenatal Cytogenetics tests in Dubai & UAE

Compare available Prenatal Cytogenetics tests, their listed prices and the information provided for each option. Test selection and preparation should be discussed with your clinician.

Tests in this category

Listed price range

2,400.00–3,000.00 AED

Clinical preparation

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Prenatal Cytogenetics test prices

Showing 1–2 of 2 matching tests.

Prenatal Cytogenetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-1366 Book Prenatal 60K Chromosomal Microarray (AF/CVS) + Karyotyping Test This diagnostic test evaluates fetal chromosomes for numerical and structural abnormalities using both microarray and karyotyping techniques.	Amniotic Fluid (AF) or Chorionic Villus Sampling (CVS)	7–9 working days	3,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosomal copy number variations (deletions/duplications)", "Aneuploidies", "Structural rearrangements"] Parameters [{"name": "Microarray Analysis", "reference_range": "Detection of copy number variations (CNVs) at ~60 kb resolution"}, {"name": "Karyotyping Analysis", "reference_range": "Detection of aneuploidies and structural rearrangements"}] Preparation ["No specific patient preparation required prior to sample collection.", "Sample collection is performed by a qualified OB/GYN in a hospital setting."] Indications ["Advanced maternal age", "Abnormal prenatal screening results", "Family history of chromosomal abnormalities", "Abnormal ultrasound findings"] Measurement technique Confirm with laboratory Codes LOINC: 81248-4 ICD-10: O35.1 Clinical summary This diagnostic test evaluates fetal chromosomes for numerical and structural abnormalities using both microarray and karyotyping techniques.
TEST-1184 Prenatal Chromosomal Aneuploidy Screening (Karyotyping + FISH for Chromosomes 13, 18, 21, X, Y) Test This diagnostic test definitively identifies numerical abnormalities of chromosomes 13, 18, 21, X, and Y using combined karyotyping and FISH.	Amniotic fluid or Chorionic villus (CVS)	15–20 days (FISH preliminary in 48–72 h)	2,400.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Numerical abnormalities of chromosomes 13, 18, 21, X, Y", "Trisomies", "Monosomy X", "Sex chromosome variations", "Mosaic patterns", "Certain structural rearrangements"] Parameters [] Preparation [] Indications ["Advanced maternal age", "Abnormal prenatal screening results", "Family history of chromosomal abnormalities", "Abnormal ultrasound findings"] Measurement technique Confirm with laboratory Codes LOINC: 34513-0 ICD-10: Z36.0 Clinical summary This diagnostic test definitively identifies numerical abnormalities of chromosomes 13, 18, 21, X, and Y using combined karyotyping and FISH.

Category overview

Prenatal Cytogenetics: overview

Investigating potential fetal anomalies requires highly precise microscopic analysis to ensure you receive the definitive reassurance you deserve. As an elite subspecialty within our Genetics department, Prenatal Cytogenetics testing meticulously evaluates fetal chromosomes for numerical or structural abnormalities from amniotic or chorionic villus samples. By leveraging state-of-the-art diagnostic technology, this advanced screening helps uncover complex chromosomal conditions, safely guiding highly specialized maternal-fetal medical care and informed family planning. Recognized for excellence in specialized reproductive diagnostics among premier diagnostic labs in Dubai and the UAE, DNA Labs guarantees strict patient confidentiality, uncompromising diagnostic accuracy, and rapid reporting for sensitive cases. Secure the critical diagnostic clarity you need—book your prenatal cytogenetics testing in UAE, coordinate a secure clinical sample collection, or consult our dedicated medical genetics experts today.

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The right diagnostic option depends on your reason for testing and individual circumstances. Check the listed specimen and timing, then confirm any preparation requirements with the ordering clinician or laboratory before collection.