Genetics
Neurological Disorders Tests in Dubai & UAE
Investigations in this area, with the specimen type, turnaround time and listed price for each option — so you and your clinician can compare before you book.
- Quality-controlled laboratory
- Home collection across the UAE
- Confidential handling of results
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Neurological Disorders investigations
All 14 investigations in this category are listed below.
| Test | What it measures | Specimen | Turnaround | Price | Book |
|---|---|---|---|---|---|
| ADGRV1 Gene Febrile Seizures, Familial, Type 4 Genetic Test TEST-4412 LOINC 94086-1 | This test identifies pathogenic mutations in the ADGRV1 gene associated with familial febrile seizures type 4. | Peripheral whole blood (EDTA) | 3–4 weeks | 2,800.00 AED | Details |
| ARID1B Gene Sequencing (NGS) Test TEST-4800 LOINC 81247-9 | This diagnostic test evaluates the ARID1B gene for pathogenic variants associated with Autosomal Dominant Intellectual Disability Type 12 and Coffin-S... | Whole Blood (EDTA), Extracted DNA, or Dried Blood Spot on FTA Card | 3 to 4 Weeks (expedited 2-week option available) | 2,800.00 AED | Details |
| Ataxia Genetic Test) TEST-3671 LOINC 92195-6 | This test identifies genetic mutations associated with various forms of hereditary ataxia. | Whole blood (EDTA), extracted DNA, or dried blood spot (FTA card) | 3–4 Weeks | 3,000.00 AED | Details |
| FIG4 Gene Amyotrophic Lateral Sclerosis Type 11 Genetic Test TEST-3771 LOINC 93942-8 | This genetic test identifies pathogenic variants in the FIG4 gene, which are linked to Autosomal Dominant Amyotrophic Lateral Sclerosis type 11. | Peripheral Blood | 3–4 Weeks | 2,800.00 AED | Details |
| FKTN Gene Walker-Warburg Syndrome Genetic Test TEST-5953 LOINC 94219-4 | This test evaluates the FKTN gene for pathogenic variants associated with Walker-Warburg syndrome using Next-Generation Sequencing. | Peripheral whole blood (3–5 mL EDTA) | 3 – 4 weeks | 2,800.00 AED | Details |
| HCRT Gene Narcolepsy DNA Test (NGS) TEST-5383 LOINC 81432-9 | This test identifies mutations in the HCRT gene, which are a known cause of narcolepsy type 1. | Peripheral whole blood | 3 – 4 weeks | 2,800.00 AED | Details |
| NLGN3 Gene Asperger Syndrome Susceptibility X-Linked Type 2 Genetic Test TEST-3818 LOINC 92872-6 | This genetic test evaluates the NLGN3 gene for variants associated with X-linked Asperger syndrome susceptibility. | Peripheral Whole Blood (EDTA) or Dry Blood Spot (FTA Card) | 3–4 Weeks | 2,800.00 AED | Details |
| OPTN Gene ALS Type 12 Genetic Test TEST-3796 LOINC 94646-4 | This genetic test evaluates the OPTN gene for pathogenic variants associated with amyotrophic lateral sclerosis type 12 (ALS12). | Peripheral Whole Blood | 3–4 weeks | 2,800.00 AED | Details |
| PAK3 Gene Mental Retardation, X-linked Type 30 Genetic Test TEST-5030 LOINC 78027-6 | This genetic test identifies pathogenic variants in the PAK3 gene associated with X-linked intellectual disability type 30. | Peripheral whole blood (EDTA), extracted DNA, or dried blood spot (FTA card) | 3–4 weeks | 2,800.00 AED | Details |
| PDE10A Gene Dyskinesia (Limb and Orofacial, Infantile-Onset) Genetic Test TEST-4227 LOINC 48808-2 | This genetic test identifies pathogenic variants in the PDE10A gene associated with severe infantile-onset limb and orofacial dyskinesia. | Peripheral whole blood, extracted DNA, or FTA card blood spot | 3 to 4 Weeks | 2,800.00 AED | Details |
| PRKCH Gene Cerebral Infarction Susceptibility Genetic Test TEST-4031 LOINC 21794-4 | This genetic test evaluates for pathogenic variants in the PRKCH gene associated with an increased risk of cerebral infarction, especially lacunar str... | Whole Blood, Extracted DNA, or FTA Card | 3–4 Weeks | 2,800.00 AED | Details |
| PRNP Gene Huntington Disease-Like Type 1 Genetic Test TEST-4521 LOINC 31208-4 | This test evaluates the PRNP gene for pathogenic variants associated with Huntington disease-like type 1. | Peripheral Blood (Whole Blood) | 3–4 Weeks | 2,800.00 AED | Details |
| VAMP1 Gene Spastic Ataxia Type 1, Autosomal Dominant Genetic Test TEST-5702 LOINC 82939-0 | This test identifies pathogenic variants within the VAMP1 gene associated with Autosomal Dominant Spastic Ataxia Type 1. | Peripheral Whole Blood | 3 – 4 Weeks | 2,800.00 AED | Details |
| VRK1 Gene Pontocerebellar Hypoplasia Type 1A Genetic Test TEST-5492 LOINC 95411-6 | This genetic test evaluates the VRK1 gene for pathogenic variants associated with Pontocerebellar Hypoplasia Type 1A. | Whole blood, extracted DNA, or dried blood spot (FTA card) | 3–4 Weeks | 2,800.00 AED | Details |
Clinical overview
About Neurological Disorders
Before your appointment
Preparation & sample collection
Follow the instructions you are given
Fasting, timing and medicine restrictions differ between investigations. The instructions for your specific request are confirmed when you book.
Bring your identification
A valid photo ID is required at collection so that your sample is matched correctly to your record.
Tell us about medicines
Prescription medicines, supplements and recent procedures can affect how an investigation is scheduled or interpreted — please mention them.
Ask before collection
If anything about preparation is unclear, contact us before your appointment. Preparation errors can affect reporting times.
Patient information
Frequently asked questions
Practical answers about Neurological Disorders testing at DNA Labs UAE. This information is general and does not replace advice from your treating clinician.
How do I choose the right Neurological Disorders test?
The correct investigation depends on what your clinician is trying to establish. Review the specimen type and turnaround time below, then confirm the choice with your treating doctor before booking.
What specimen is required?
Specimen requirements are listed for each investigation. If a request involves more than one sample type, our team will confirm what is needed at the time of booking.
Do you offer home sample collection in Dubai and the UAE?
Yes. Home collection can be arranged across Dubai and the wider UAE. Availability and appointment windows vary by location, so please confirm when you book.
How long do results take?
Turnaround depends on the investigation and the method used. The expected reporting time is confirmed with you before collection.
Is there anything I need to do before sample collection?
Some investigations require fasting, a specific collection time, or avoiding certain medicines or activities. Preparation details are shared when you book — please follow them and ask if anything is unclear.
How will I receive my report?
Reports are issued as secure digital documents and can be shared with your referring clinician on request. Please review results with a qualified clinician who can interpret them in context.
About this clinical information
The information on this Neurological Disorders page describes laboratory investigations in general terms. It is written to help you understand what an investigation involves — it is not a diagnosis and it is not a substitute for advice from your treating clinician.
- Investigation names, specimen types and listed prices are reviewed against laboratory records.
- Preparation guidance is indicative — confirm test-specific instructions before collection.
- Content is updated when investigations, methods or reporting formats change.
- Results are released to the patient and, on request, shared with the referring clinician.
Medical disclaimer: This page is for general information and education only. It is not medical advice, diagnosis or treatment, and it does not replace a consultation with a qualified healthcare professional. Always seek the advice of your doctor or another qualified provider with any questions about a medical condition or before ordering a test.
We're here to help
Need help choosing a Neurological Disorders test?
Tell us what your clinician has requested and we'll confirm availability, price, preparation and the most convenient collection option — including home collection in Dubai and across the UAE.
- Home collection available across the UAE
- Digital reports delivered securely
- Confidential handling of every request
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