Test Price
2,800 AED✅ Home Collection Available
MT-TR Mitochondrial Encephalomyopathy Genetic Test (NGS) in UAE – 2,800 AED
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Certified Lab (Cert: INT/EGQ/2509DA/3139).
- Premium Home Collection: Iso-Certified Cold-Chain Home Blood Draw (8 AM – 11 PM) & VIP Mobile Phlebotomy.
- Post-Test Clinical Guidance: Complimentary telephone interpretation with a genetics specialist.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
- Legal Compliance: Full adherence to UAE 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.
- Test Name: MT-TR Mitochondrial Encephalomyopathy NGS.
- Price: 2,800 AED (All inclusive – home collection, sequencing, clinical report).
- Turnaround Time: 3 to 4 weeks.
- Sample Type: Whole Blood (2–3 mL) – VIP Home Phlebotomy available daily 8 AM – 11 PM.
- DHA Facility License: 1143
Test Overview & Methodology
This next-generation sequencing (NGS) test screens the entire coding region of the MT-TR gene for pathogenic variants linked to mitochondrial encephalomyopathy, including MELAS (Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like episodes). Using Illumina NovaSeq technology, the assay detects single nucleotide variants, insertions, deletions, and copy number variations with >99.9% sensitivity across the gene. Bioinformatics analysis follows ACMG guidelines. This test replaces legacy Sanger sequencing of limited hotspots, offering broader coverage and higher diagnostic yield.
| Feature | Our MT-TR NGS Test | Standard Single‑Gene Sequencing |
|---|---|---|
| Methodology | NGS (Illumina NovaSeq) – full gene, CNV detection | Sanger sequencing of limited hotspots |
| Sensitivity | >99.9% for all coding variants | ~85% in targeted regions |
| Turnaround Time | 3 to 4 weeks | 4 to 6 weeks |
| Bioinformatics | ACMG guidelines, deep variant analysis | Manual curation, limited pipelines |
| Price (AED) | 2,800 | 3,200 |
Physician Insight & Safety Protocols
“A positive MT-TR mutation confirms mitochondrial pathology, but clinical correlation with encephalopathy, lactic acidosis, and stroke-like episodes remains paramount. Genetic results should never replace urgent metabolic or neurological evaluation; they guide long‑term surveillance and family planning. We are here to translate complex data into actionable care.” — Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
⚠️ Medication Advisory
Do not discontinue any prescribed anticonvulsants, coenzyme Q10, or carnitine supplements without consulting your treating neurologist. Abrupt withdrawal can trigger metabolic decompensation. This test is elective – it does not replace acute medical care.
Safety Exclusion Criteria & Red Flags
- Collection is contraindicated during acute stroke‑like episodes; stabilise patient first.
- Blood transfusion within 2 weeks may cause donor DNA contamination – postpone draw.
- Severe hemolysis or clotting invalidates the sample; our phlebotomists strictly adhere to pre‑analytical SOPs.
- For minors (<18 years), a legal guardian must provide consent and be present, in line with Federal Decree-Law No. 4 of 2016 on Medical Liability.
- ER Red Flags: Sudden severe headache with vomiting, new‑onset seizures, acute weakness, or loss of consciousness require immediate emergency care – this test is elective, not acute.
Patient FAQ & Clinical Guidance
1. What does the MT-TR gene test diagnose?
This NGS assay identifies pathogenic MT-TR variants causing mitochondrial encephalomyopathy, lactic acidosis and stroke‑like episodes (MELAS), as well as isolated myopathy, enabling precise molecular diagnosis. It is a targeted genetic test, not a whole exome screen.
2. How is the test performed and what is the turnaround time?
Our certified phlebotomist collects 2–3 mL of whole blood during a home visit (8 AM – 11 PM, daily). The sample is transported under temperature‑controlled cold chain to our CAP‑accredited lab. Results are typically available within 3–4 weeks and include a telephonic interpretation with a genetics specialist.
3. Is this genetic test covered by UAE health insurance?
Most UAE insurers cover medically necessary genetic testing for mitochondrial disorders. We verify your benefits via WhatsApp and assist with pre‑authorization using ICD‑10‑CM codes E88.4 and Z13.79. Direct billing is available for selected networks.
4. Are there any risks or side effects of the blood draw?
The blood draw is minimally invasive; risks include minor bruising, discomfort, or lightheadedness. Our phlebotomists follow strict safety protocols. If you have a bleeding disorder or take anticoagulants, please inform the phlebotomist in advance.
UAE Regulatory & Data Privacy Adherence
DNA Labs UAE operates under DHA Facility License No. 1143. All genetic data is processed in strict compliance with 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 information is encrypted, access‑controlled, and never shared without explicit consent. Clinical safety and informed consent protocols adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability.
Clinical & Logistical Metadata
| Test Name | MT-TR Mitochondrial Encephalomyopathy Genetic Test (NGS) |
| Price (AED) | 2,800 |
| Turnaround Time | 3 to 4 weeks |
| Sample Type / Matrix | Whole Blood (2–3 mL) – VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Available daily from 8 AM to 11 PM) |
| Methodology Used | Next-Generation Sequencing (NGS) – Illumina NovaSeq, full gene coverage, CNV detection |
| ICD-10-CM Code | E88.4, Z13.79 |
| LOINC Code | 101234-5 |
| DHA Facility License & Address | DHA License No. 1143 – Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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