Genetic Neurological Disorders tests in Dubai & UAE

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

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Listed price range

2,800.00 AED

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Genetic Neurological Disorders test prices

Showing 1–5 of 5 matching tests.

Genetic Neurological Disorders diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-4639 CNKSR2 Gene Nonsyndromic Intellectual Disability (CNKSR2‑Related) Genetic Test This genetic test analyzes the CNKSR2 gene for variants associated with X-linked nonsyndromic intellectual disability.	Peripheral Whole Blood (EDTA), FTA Card, or Extracted DNA	3 – 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the CNKSR2 gene", "Single-nucleotide variants (SNVs)", "Small deletions/insertions (indels)", "Copy number variants (CNVs)"] Parameters [] Preparation ["Pre-genetic counselling session is mandatory", "No fasting required", "Avoid concomitant use of DNA-degrading substances like heparin"] Indications ["Diagnosis of X-linked nonsyndromic intellectual disability", "Genetic counselling for families with affected individuals", "Recurrence risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 81274-5 ICD-10: Z13.71 Clinical summary This genetic test analyzes the CNKSR2 gene for variants associated with X-linked nonsyndromic intellectual disability.
TEST-4826 DEAF1 Gene Genetic Test for Autosomal Dominant Intellectual Disability Type 24 (MRD24) This test identifies pathogenic variants within the DEAF1 gene associated with Autosomal Dominant Intellectual Disability Type 24 (MRD24).	Peripheral whole blood (EDTA), extracted DNA, or dried blood spot	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["DEAF1 gene variants", "Single-nucleotide variants", "Small insertions/deletions (indels)", "Copy-number variants (CNVs)"] Parameters [] Preparation ["No specific fasting required.", "Inform the lab of any current medications."] Indications ["Suspected diagnosis of Autosomal Dominant Intellectual Disability Type 24 (MRD24)", "Family history of MRD24", "Genetic counseling for recurrence risk assessment", "Prenatal or preimplantation genetic diagnosis planning"] Measurement technique Confirm with laboratory Codes LOINC: 82107-4 ICD-10: Q87.8 Clinical summary This test identifies pathogenic variants within the DEAF1 gene associated with Autosomal Dominant Intellectual Disability Type 24 (MRD24).
TEST-4959 MAN1B1 Gene Mental Retardation, Autosomal Recessive Type 15 Genetic Test This test detects pathogenic variants in the MAN1B1 gene associated with autosomal recessive intellectual disability type 15.	Peripheral whole blood (EDTA tube) or saliva (Oragene collection kit)	3 – 4 Weeks (21 – 28 calendar days 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 MAN1B1 gene", "Alpha-1,2-mannosidase enzyme function (indirectly)"] Parameters [] Preparation ["No specific fasting required", "No medication or diet restrictions"] Indications ["Suspected autosomal recessive intellectual disability type 15", "Evaluation of global developmental delay with associated features"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: F78 Clinical summary This test detects pathogenic variants in the MAN1B1 gene associated with autosomal recessive intellectual disability type 15.
TEST-5874 PEX10 Gene Zellweger Syndrome Spectrum Genetic Test This genetic test identifies pathogenic variants in the PEX10 gene to confirm a clinical diagnosis of Zellweger Spectrum Disorder.	Blood (Whole Blood, EDTA), Extracted DNA, or FTA Card	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the PEX10 gene", "Peroxisome biogenesis"] Parameters [] Preparation ["Complete pre-test genetic counseling session", "Share medication or supplement lists with primary physician"] Indications ["Confirmation of clinical diagnosis of Zellweger Spectrum Disorder", "Familial genetic counseling"] Measurement technique Confirm with laboratory Codes LOINC: 81313-5 ICD-10: E71.510 Clinical summary This genetic test identifies pathogenic variants in the PEX10 gene to confirm a clinical diagnosis of Zellweger Spectrum Disorder.
TEST-4573 TMEM237 Gene Joubert Syndrome Type 14 Genetic Test This genetic test evaluates the TMEM237 gene for mutations associated with Joubert syndrome type 14.	Whole blood (EDTA), extracted DNA, or FTA card (peripheral blood)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TMEM237 gene sequence", "Copy Number Variants (CNV) in TMEM237"] Parameters [] Preparation ["Genetic counselling is mandatory prior to sample collection"] Indications ["Diagnosis of Joubert syndrome type 14", "Genetic counselling for families with Joubert syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 57555-2 ICD-10: Q04.3 Clinical summary This genetic test evaluates the TMEM237 gene for mutations associated with Joubert syndrome type 14.

Category overview

Genetic Neurological Disorders: overview

Navigating a family history of progressive movement disorders, early cognitive decline, or severe neuropathies warrants proactive, empowering insights to protect your long-term brain health. Representing a critical pillar of our advanced Genetics services, testing for Genetic Neurological Disorders comprehensively evaluates your DNA for inherited mutations linked to conditions like Huntington's disease, inherited ataxias, or familial ALS. By leveraging state-of-the-art sequencing technology, this expansive molecular profiling delivers the critical clarity needed to assess hereditary risks, safely guiding customized neurological monitoring, early therapeutic interventions, and informed family planning. Consistently ranked among the premier diagnostic labs in Dubai and the UAE, DNA Labs ensures strict patient confidentiality, exceptional analytical precision, and prompt, reliable reporting. Prioritize your neurological future—book your genetic neurological disorders testing in UAE, arrange a secure home sample collection, or connect with our specialized genetic counselors.

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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.