Genetics
Neurological Genetic 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.
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- Home collection across the UAE
- Confidential handling of results
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Neurological Genetic Disorders investigations
All 21 investigations in this category are listed below.
| Test | What it measures | Specimen | Turnaround | Price | Book |
|---|---|---|---|---|---|
| AARS1 Gene (CMT2N) Genetic Test TEST-4036 LOINC 21636-6 | This test evaluates the AARS1 gene for pathogenic variants associated with autosomal dominant axonal Charcot-Marie-Tooth disease type 2N (CMT2N). | Peripheral whole blood | 3 to 4 weeks | 2,800.00 AED | Details |
| CACNA1S Gene Hypokalemic Periodic Paralysis Type 1 Genetic Test TEST-4546 LOINC 21636-6 | This genetic test identifies pathogenic variants in the CACNA1S gene, confirming the diagnosis of hypokalemic periodic paralysis type 1. | Whole blood (EDTA), extracted DNA, or dried blood spot (FTA card) | 3–4 weeks (21–28 calendar days) | 2,800.00 AED | Details |
| COL4A2 Gene Porencephaly Type 2 Genetic Test TEST-5605 LOINC 81247-9 | This genetic test identifies pathogenic variants in the COL4A2 gene, which are associated with familial porencephaly type 2 and cerebrovascular malfor... | Peripheral Whole Blood / Extracted DNA / FTA Card | 3-4 Weeks | 2,800.00 AED | Details |
| CPLANE1 Gene (Joubert Syndrome Type 17) Genetic Test TEST-4658 LOINC 48006-4 | This test identifies pathogenic variants in the CPLANE1 gene associated with Joubert syndrome type 17. | Peripheral Whole Blood (EDTA) or FTA Card Blood Spot | 21–28 Business Days (3–4 Weeks) | 2,800.00 AED | Details |
| DNAL4 Gene (Mirror Movements Type 3) Genetic Test TEST-5004 LOINC 94825-7 | This test identifies pathogenic variants in the DNAL4 gene associated with congenital mirror movements type 3 (CMM3). It provides molecular confirmati... | Peripheral blood, FTA card, or extracted DNA | 3-4 weeks | 2,800.00 AED | Details |
| DST Gene Neuropathy, Hereditary Sensory and Autonomic Type 6 (HSAN6) Genetic Test TEST-5376 LOINC 86238-5 | This genetic test evaluates the DST gene for pathogenic variants associated with Hereditary Sensory and Autonomic Neuropathy Type 6 (HSAN6). It provid... | Peripheral whole blood (FTA card or venous) | 3–4 Weeks | 2,800.00 AED | Details |
| GBA2 Gene Cerebellar Ataxia with Spasticity Genetic Test TEST-3970 LOINC 82327-0 | This test identifies pathogenic variants in the GBA2 gene associated with autosomal recessive cerebellar ataxia with spasticity (SPG46/SCAR17). | Peripheral Whole Blood or FTA Card | 3 – 4 Weeks | 2,800.00 AED | Details |
| KCNC1 Gene Epilepsy, Progressive Myoclonic Type 7 Genetic Test TEST-4445 LOINC 93755-4 | This genetic test identifies pathogenic variants in the KCNC1 gene, confirming a diagnosis of progressive myoclonic epilepsy type 7 (EPM7). | Whole blood (EDTA), extracted DNA, or dried blood spot (FTA card) | 14–21 Business Days | 2,800.00 AED | Details |
| KCNJ10 Gene SESAME Syndrome Genetic Test TEST-5684 LOINC 82146-7 | This test sequences the KCNJ10 gene to identify pathogenic variants associated with SESAME syndrome. | Whole Blood (Peripheral) | 3 to 4 Weeks (21–28 calendar days) | 2,800.00 AED | Details |
| KIF7 Gene Acrocallosal Syndrome Genetic Test TEST-3726 LOINC 60511-6 | This genetic test identifies pathogenic mutations, including deletions and duplications, in the KIF7 gene associated with acrocallosal syndrome. | Whole Blood (EDTA), Buccal Swab, or Extracted DNA | 3–4 Weeks | 2,800.00 AED | Details |
| NDUFAF1 Gene Leigh Syndrome Genetic Test TEST-4716 LOINC 101484-1 | This test analyzes the NDUFAF1 gene to detect pathogenic variants associated with Leigh syndrome, a severe neurological disorder. | Whole Blood (EDTA) | 3–4 Weeks | 2,800.00 AED | Details |
| NDUFS3 Gene (Leigh Syndrome) Genetic Test TEST-4725 LOINC 55233-1 | This genetic test identifies mutations in the NDUFS3 gene associated with Leigh syndrome. | Blood, Extracted DNA, FTA Card (one drop blood) | 3 to 4 Weeks | 2,800.00 AED | Details |
| PAFAH1B1 Gene Lissencephaly Type 1 (LIS1) Genetic Test TEST-2638 LOINC 89820-2 | This test identifies pathogenic variants in the PAFAH1B1 gene associated with classic lissencephaly type 1. | Peripheral whole blood (EDTA), extracted DNA, or dried blood spot (FTA card) | 3 to 4 weeks | 2,800.00 AED | Details |
| PLP1 Gene Pelizaeus-Merzbacher Disease Genetic Test TEST-5452 LOINC 62138-2 | This test evaluates the PLP1 gene for pathogenic variants associated with Pelizaeus-Merzbacher disease. | Peripheral Blood | 3–4 Weeks | 2,800.00 AED | Details |
| PRNP Gene Gerstmann-Sträussler Disease Genetic Test TEST-4444 LOINC 21656-1 | This test evaluates the PRNP gene for mutations associated with Gerstmann-Sträussler-Scheinker disease. | Peripheral Whole Blood | 3–4 Weeks | 2,800.00 AED | Details |
| RNASEH2B Gene Aicardi-Goutières Syndrome Type 2 Genetic Test TEST-3722 LOINC 83267-5 | This test evaluates the RNASEH2B gene for pathogenic variants associated with Aicardi-Goutières Syndrome Type 2 (AGS2). It uses Next-Generation Sequen... | Blood (Whole Blood, Serum, or Plasma) | 3–4 weeks | 2,800.00 AED | Details |
| SEPT9 Gene Hereditary Neuralgic Amyotrophy (HNA) Genetic Test TEST-3807 LOINC 77418-8 | This genetic test analyzes the SEPT9 gene for mutations associated with Hereditary Neuralgic Amyotrophy (HNA). | Peripheral whole blood collected in EDTA tube | 3–4 weeks | 2,800.00 AED | Details |
| SLC13A5 Gene Early Infantile Epileptic Encephalopathy Type 25 (EIEE25) Genetic Test TEST-4253 LOINC 87153-8 | This genetic test identifies pathogenic variants in the SLC13A5 gene associated with early infantile epileptic encephalopathy type 25 (EIEE25). | Peripheral Whole Blood or Dried Blood Spot (FTA Card) | 3 to 4 weeks | 2,800.00 AED | Details |
| SLC16A2 Gene Allan-Herndon-Dudley Syndrome Genetic Test TEST-3736 LOINC 29564-7 | This genetic test evaluates the SLC16A2 gene for mutations associated with Allan-Herndon-Dudley syndrome. | Peripheral Whole Blood | 3–4 Weeks | 2,800.00 AED | Details |
| TOR1A Gene (DYT1) Next‑Generation Sequencing (Genetic Test TEST-4239 LOINC 94760-6 | This genetic test identifies mutations in the TOR1A gene, specifically the GAG deletion, associated with early-onset primary torsion dystonia (DYT1). | Peripheral Whole Blood or Dried Blood Spot (FTA Card) | 21–28 Calendar Days | 2,800.00 AED | Details |
| TWNK Gene Perrault Syndrome Type 5 Next-Generation Sequencing (NGS) Genetic Test TEST-5479 LOINC 21636-6 | This test identifies pathogenic variants in the TWNK gene, confirming a diagnosis of Perrault syndrome type 5. | Whole Blood (3–5 mL), Buccal Swab, or FTA Card | 3–4 Weeks | 2,800.00 AED | Details |
Clinical overview
About Neurological Genetic 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 Genetic 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 Genetic 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 Genetic 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.
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- Home collection available across the UAE
- Digital reports delivered securely
- Confidential handling of every request
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