Genetic Screening tests in Dubai & UAE

Compare available Genetic Screening 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

1,000.00–2,800.00 AED

Clinical preparation

Confirm test-specific instructions with your clinician or laboratory.

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Genetic Screening test prices

Showing 1–4 of 4 matching tests.

Genetic Screening diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-1487 Huntington Disease Mutation Screening Test This test evaluates the number of CAG repeats in the HTT gene to diagnose or predict Huntington disease.	2–5 mL peripheral blood (EDTA tube)	7 days from sample receipt	1,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["CAG trinucleotide repeat expansion", "HTT gene mutation"] Parameters [{"name": "CAG Repeat Count (Allele 1)", "reference_range": "Normal: Preparation ["No fasting needed", "Valid doctor’s prescription required (exceptions: DHA-approved surgery clearance, pregnancy screening, or international travel fitness)", "Guardian consent mandatory for minors (Federal Law No. 2 of 2019)"] Indications ["Diagnostic confirmation of Huntington disease", "Predictive testing for individuals with family history", "Pre-test counselling required (exceptions apply)", "Family risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 58993-1 ICD-10: G10, Z13.79, Z15.89 Clinical summary This test evaluates the number of CAG repeats in the HTT gene to diagnose or predict Huntington disease.
TEST-3560 NHS Gene Cataract, X‑linked Genetic Test This test analyzes the NHS gene for pathogenic variants associated with Nance-Horan syndrome, an X-linked disorder causing congenital cataract, dental anomalies, and intellectual d...	Whole Blood (EDTA/NaCitrate), Extracted DNA, or FTA Card	3–4 weeks from sample receipt	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the NHS gene", "Single-nucleotide variants", "Indel variants", "Copy-number changes"] Parameters [] Preparation ["Fasting is not required.", "Patients on anticoagulants must inform the phlebotomist."] Indications ["Diagnosis of Nance-Horan syndrome", "Carrier screening in families with affected individuals", "Prenatal diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 57998-1 ICD-10: Q12.0 Clinical summary This test analyzes the NHS gene for pathogenic variants associated with Nance-Horan syndrome, an X-linked disorder causing congenital cataract, dental anomalies, and intellectual disability.
TEST-1190 Preimplantation Genetic Screening (PGS) per Embryo Test This test evaluates blastocyst biopsies for chromosomal aneuploidies using NGS and Chromosomal Microarray.	Embryo biopsy (blastocyst)	1-2 business days	1,600.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosomal aneuploidy", "Segmental imbalances"] Parameters [] Preparation [] Indications ["Patients undergoing In Vitro Fertilization (IVF)", "Screening embryos for chromosomal abnormalities prior to transfer"] Measurement technique Confirm with laboratory Codes LOINC: 82688-9 ICD-10: Z31.49 Clinical summary This test evaluates blastocyst biopsies for chromosomal aneuploidies using NGS and Chromosomal Microarray.
TEST-2946 PREIMPLANTATION GENETIC SCREENING (PGS) Test This diagnostic test evaluates embryos for chromosomal abnormalities using Next Generation Sequencing (NGS) prior to IVF transfer.	Embryo biopsy cells	7 business days	1,900.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosomal copy number variations (aneuploidy)", "Whole chromosome analysis"] Parameters [] Preparation ["Complete mandatory Preimplantation Genetic Screening Consent Form (Form 23) prior to collection.", "Embryo biopsy performed by IVF clinic under sterile conditions."] Indications ["Recurrent miscarriages", "Advanced maternal age", "Previous IVF failures", "Known genetic disorders"] Measurement technique Confirm with laboratory Codes LOINC: 89054-9 ICD-10: O35.0XX0, Z31.441, Z13.79 Clinical summary This diagnostic test evaluates embryos for chromosomal abnormalities using Next Generation Sequencing (NGS) prior to IVF transfer.

Category overview

Genetic Screening: overview

Safeguarding your future and your family's health begins with proactive, empowering insights that bring unparalleled reassurance before symptoms ever appear. Integrated into our comprehensive preventative health services, Genetic Screening evaluates your DNA to assess carrier status for common hereditary conditions or to determine your personal risk for specific diseases. Utilizing advanced diagnostic technology, this vital preventative profiling helps uncover hidden molecular risks, offering the definitive clarity needed to safely guide personalized lifestyle adjustments, early medical monitoring, and informed reproductive decisions. Highly regarded for preventative diagnostic excellence among top diagnostic labs in the UAE, DNA Labs guarantees absolute patient confidentiality, uncompromising diagnostic accuracy, and prompt turnaround times. Prioritize your lifelong wellness—schedule your genetic screening in UAE, coordinate a seamless home sample collection, or connect with our specialized wellness team today.

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Use the test details as a conversation starter

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.