Test Price
2,800 AED✅ Home Collection Available
MT-ND5 Gene Genetic Test for Leigh Syndrome (Mitochondrial Complex I Deficiency) in UAE – 2,800 AED
Executive Summary & Core Metrics
The MT-ND5 gene NGS test provides definitive diagnosis of Leigh syndrome caused by mitochondrial complex I deficiency, with diagnostic sensitivity exceeding 99.9% through ISO‑accredited next‑generation sequencing. Core service guarantees include:
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing.
- Premium Logistics: VIP Mobile Phlebotomy and Temperature‑Controlled Cold‑Chain Home Collection, available daily 8 AM – 11 PM.
- Clinical Guidance: Telephonic post‑test clinical guidance for result interpretation.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
This test uses next‑generation sequencing (NGS) to comprehensively examine the entire MT‑ND5 mitochondrial gene for pathogenic variants associated with Leigh syndrome. NGS offers superior sensitivity for single‑nucleotide variants and small insertions/deletions compared to traditional Sanger sequencing, and enables full‑gene coverage in a single assay.
| Feature | Our Test (NGS MT-ND5) | Closest Alternative (Sanger Sequencing) |
|---|---|---|
| Precision | 99.9% sensitivity for single‑nucleotide variants and small indels | High accuracy but restricted to exonic regions; may miss deep intronic changes |
| Method | Next Generation Sequencing (NGS) – full gene coverage | Sanger sequencing, exon by exon |
| Turnaround Time | 3–4 weeks | 4–6 weeks |
Physician Insight & Safety Protocols
“This genetic test provides critical insight into mitochondrial complex I deficiency, but results must be interpreted in the full clinical context, including MRI findings and biochemical markers. Genetic counselling before and after testing is mandatory to understand inheritance patterns and implications for family members.”
— Lina Osama Zaki Quteineh, Consultant Medical Genetics (DHA Registration ID: 9294403)
Advisory – Medication & Sample Safety
⚠️ Do not discontinue any prescribed medication without consulting your physician. Inform the phlebotomist if you are taking anticoagulants; do not stop medications abruptly.
Exclusion Criteria & Safety Red Flags
- Inability to provide a viable blood or DNA sample according to protocol.
- Patients with known bleeding disorders should consult their physician prior to blood draw.
- Emergency Red Flags: If the patient experiences rapid neurological deterioration, seizures, or respiratory distress, seek immediate emergency care – do not wait for test results.
Patient FAQ & Clinical Guidance
1. What is the MT-ND5 gene NGS test used for?
The MT-ND5 gene NGS test diagnoses Leigh syndrome due to mitochondrial complex I deficiency by sequencing the entire MT-ND5 gene with high sensitivity. It identifies pathogenic mutations linked to this severe neurological disorder, enabling precise medical management and family screening.
2. Why choose this test in the UAE under current regulatory standards?
Our MT-ND5 test complies with UAE federal genomics regulations, uses ISO 9001:2015 certified processes, and offers home collection with cold‑chain integrity for reliable mitochondrial DNA analysis. Your sample is handled in accordance with UAE data protection and health information privacy laws.
3. How does home collection work and what is the turnaround time?
Home collection is performed by a licensed phlebotomist between 8 AM and 11 PM, with VIP mobile service using EDTA blood or FTA card. Results are delivered in 3–4 weeks after the lab receives the sample. You will receive telephonic clinical guidance to interpret the results.
UAE Regulatory & Data Privacy Adherence
Our Commitment to Compliance
All clinical data handling and processing strictly adhere to Federal Decree‑Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. Patient consent and clinical safety follow the provisions of Federal Decree‑Law No. 4 of 2016 on Medical Liability. DNA Labs UAE is fully compliant with DHA Facility License No. 1143 (Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE). ISO 9001:2015 Certification: INT/EGQ/2509DA/3139.
Clinical & Logistical Metadata
| Test Name | MT-ND5 Gene Next Generation Sequencing (NGS) for Leigh Syndrome |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3–4 weeks |
| Sample Type / Matrix | Peripheral whole blood (EDTA) or DNA sample (FTA card acceptable) |
| Methodology Used | Next Generation Sequencing (NGS) – full gene coverage |
| ICD-10-CM Code | G31.82 (Leigh syndrome) |
| LOINC Code | 93634-8 (Mitochondrial genome sequencing) |
| DHA Facility License & Laboratory Address | DHA License No. 1143 – Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE. Corporate Branding: DNA Labs UAE |
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Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians