Fragile X Syndrome tests in Dubai & UAE

Compare available Fragile X Syndrome 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

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Fragile X Syndrome test prices

Showing 1–3 of 3 matching tests.

Fragile X Syndrome diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-4492 FMR1 Gene (Fragile X Syndrome) Genetic Test This test comprehensively analyzes the FMR1 gene for CGG repeat expansions, methylation status, and rare sequence variants associated with Fragile X syndrome.	Whole Blood (EDTA), Extracted DNA, or Dried Blood Spot (FTA Card)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["CGG repeat expansions in the FMR1 gene", "Methylation status of the FMR1 promoter", "Rare sequence variants in the FMR1 gene"] Parameters [] Preparation ["No food or medication restrictions apply.", "A detailed clinical history including developmental milestones and family pedigree is required.", "A mandatory genetic counselling session is required before sample collection."] Indications ["Individuals with intellectual disability or autism", "Individuals with a family history of Fragile X syndrome", "Carrier screening for parents planning pregnancy", "Children showing developmental delay", "Adults with tremor/ataxia of unknown cause"] Measurement technique Confirm with laboratory Codes LOINC: 21771-5 ICD-10: Q99.2 Clinical summary This test comprehensively analyzes the FMR1 gene for CGG repeat expansions, methylation status, and rare sequence variants associated with Fragile X syndrome.
TEST-4421 FMR1 Gene (Fragile X Tremor/Ataxia Syndrome) Genetic Test This genetic test analyzes the FMR1 gene for CGG repeat expansions to diagnose Fragile X-associated tremor/ataxia syndrome (FXTAS) in premutation carriers.	Whole Blood, Extracted DNA, or DNA FTA Card	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["CGG trinucleotide repeat number in the FMR1 gene", "AGG interruption patterns", "Methylation status of the FMR1 gene"] Parameters [{"name": "CGG Repeat Number", "reference_range": "< 55 (Normal), 55-200 (Premutation), >200 (Full Mutation)"}, {"name": "AGG Interruption", "reference_range": "Detected / Not Detected"}, {"name": "Methylation Status", "reference_range": "Methylated / Unmethylated"}] Preparation ["No specific drug or supplement avoidance required", "Continue prescribed medications unless advised otherwise by your doctor"] Indications ["Adults with progressive intention tremor, cerebellar ataxia, parkinsonism, or cognitive decline", "Individuals with a family history of Fragile X disorders", "Neurology referral recommended"] Measurement technique Confirm with laboratory Codes LOINC: 80135-6 ICD-10: Z13.79 Clinical summary This genetic test analyzes the FMR1 gene for CGG repeat expansions to diagnose Fragile X-associated tremor/ataxia syndrome (FXTAS) in premutation carriers.
TEST-1463 Karyotyping for Fragile X Syndrome Detection Test This test evaluates the X chromosome for a specific fragile site (Xq27.3) associated with Fragile X Syndrome using cytogenetic analysis.	Peripheral Whole Blood	7–10 days	1,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Cytogenetic fragile site induction", "Chromosomal breakage and structural rearrangements"] Parameters [] Preparation ["Disclose all current medications, supplements, and herbal remedies prior to sample collection.", "Continue all prescribed medications unless advised otherwise by a physician."] Indications ["Diagnosis of Fragile X Syndrome", "Carrier screening for reproductive planning", "Family history of Fragile X Syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 34542-2 ICD-10: Q99.2 Clinical summary This test evaluates the X chromosome for a specific fragile site (Xq27.3) associated with Fragile X Syndrome using cytogenetic analysis.

Category overview

Fragile X Syndrome: overview

Addressing a child's developmental delays, autism spectrum behaviors, or learning challenges demands compassionate, highly specific diagnostic care to unlock the best possible support. As an elite subspecialty in our Genetics services, Fragile X Syndrome testing focuses specifically on full mutations in the FMR1 gene, the leading inherited cause of intellectual disability. Utilizing cutting-edge molecular technology, this crucial genomic screening confirms the diagnosis, providing the definitive data needed to safely guide highly customized pediatric interventions, tailored educational strategies, and informed family planning. Consistently trusted by pediatricians across the top diagnostic labs in the UAE, DNA Labs guarantees absolute patient confidentiality, exceptional analytical precision, and incredibly efficient reporting. Empower your child’s developmental journey—schedule your Fragile X syndrome testing in UAE, coordinate a comfortable home sample collection, or reach out to our dedicated genetic counselors.

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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.