Test Price
3,000 AED✅ Home Collection Available
Mitochondrial Genome Sequencing Analysis in UAE | 3,000 AED | DHA Licensed Lab 1143
Executive Summary & Core Metrics
Mitochondrial Genome Sequencing is a high-complexity molecular diagnostic analysis offered exclusively by DNA Labs UAE at our DHA-licensed facility (License No. 1143) in Dubai Healthcare City. The test achieves a 99.9% diagnostic sensitivity through deep whole-mitochondrial genome coverage using Next-Generation Sequencing (NGS) with orthogonal Sanger confirmation. Our ISO 9001:2015 certified laboratory ensures rigorous quality control. The service includes VIP mobile phlebotomy with temperature-controlled cold-chain transport (available daily 8 AM to 11 PM), a comprehensive clinical report, and a post-test telephonic consultation with a genetics specialist. Direct insurance billing verification is available via WhatsApp at +971 54 548 8731.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity – ISO Certified Processing.
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection.
- Clinical Guidance: Telephonic Post-Test Clinical Interpretation & Genetic Counselling.
- Insurance: Direct Billing Verification via WhatsApp at +971 54 548 8731.
Test Overview & Methodology
This comprehensive analysis sequences the entire 16.6 kb mitochondrial genome using Next-Generation Sequencing (NGS) to identify pathogenic single nucleotide variants (SNVs), small insertions/deletions (indels), large structural rearrangements, and heteroplasmy levels down to 1%. The test is clinically indicated for investigating suspected mitochondrial disorders, evaluating oncologic risk associated with mitochondrial dysfunction, and assessing rheumatologic conditions with unexplained metabolic involvement. All findings are interpreted by a board-certified Consultant Medical Geneticist.
| Feature | Our Test (DHA‑Certified Lab) | Closest Alternative |
|---|---|---|
| Precision | Full mtDNA genome at >1000x depth, heteroplasmy detection ≥1% | Limited target panels or single‑gene assays |
| Method | NGS with Sanger confirmation and expert bioinformatic curation | PCR‑RFLP or Sanger sequencing of selected hotspots |
| Speed | Turnaround time: 21 – 28 Business Days | Often 6 – 8 weeks |
Physician Insight & Safety Protocols
"Mitochondrial genome sequencing provides a unique window into the energetic machinery of our cells. As a Consultant Medical Geneticist, I correlate every detected variant—whether a homoplasmic mutation or a low-level heteroplasmy—with the patient's full clinical presentation. This test is invaluable for diagnosing complex multisystem disorders, but its power lies in expert interpretation. Our commitment at DNA Labs UAE is to deliver not just data, but meaningful clinical clarity."
– Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
Medication Advisory & Safety Considerations
⚠ Medication Advisory: Do not alter, stop, or adjust any prescribed medications—including mitochondrial supplements, anticonvulsants, or anticoagulants—without direct consultation with your treating physician. This diagnostic test is designed to inform, not replace, your existing medical management plan. Please bring a complete list of your current medications to the phlebotomy appointment.
Exclusion Criteria & Emergency Indicators
Phlebotomy Contraindications
- Exclusion Criteria: Sample collection via phlebotomy should be deferred in patients presenting with active febrile illness, severe uncorrected coagulopathy (INR > 3.0), or platelet count < 20,000/µL. If any of these apply, please reschedule following consultation with your primary care physician.
ER Red Flags – Seek Immediate Medical Attention
- Sudden onset of ptosis, ophthalmoplegia, or unexplained seizure activity.
- Exercise intolerance accompanied by metabolic acidosis or respiratory difficulty.
- Unexplained stroke-like episodes or loss of consciousness.
Patient FAQ & Clinical Guidance
1. What is the clinical utility of mitochondrial genome sequencing?
Snippet-ready: This test sequences the entire mitochondrial DNA to detect pathogenic point mutations, deletions, and heteroplasmy levels associated with mitochondrial encephalomyopathies, Leigh syndrome, MELAS, MERRF, Leber hereditary optic neuropathy (LHON), and certain oncologic or rheumatologic conditions. It provides a definitive molecular diagnosis to guide management and family counselling.
2. How is the sample collected for this genetic test?
Snippet-ready: No fasting or special preparation is required. A trained phlebotomist will visit your home within the designated VIP mobile phlebotomy window (8 AM to 11 PM daily) to collect one peripheral whole blood sample using an ISO-certified cold-chain kit. The specimen is transported directly to our DHA-licensed laboratory in Dubai Healthcare City.
3. What does the test price cover and is insurance billed directly?
Snippet-ready: The 3,000 AED fee includes VIP home phlebotomy, full NGS sequencing and Sanger confirmation, a detailed clinical report, and a telephonic consultation with a genetics specialist. We offer direct billing to major UAE insurance providers. To verify your specific coverage, send a photo of your insurance card via WhatsApp to +971 54 548 8731.
4. How are results reported and delivered?
Snippet-ready: Results are typically available within 21 to 28 business days. You will receive a secure electronic PDF report containing all detected variants, heteroplasmy percentages, pathogenicity classifications per ACMG guidelines, and clinical interpretations. A telephonic disclosure session is scheduled with our Consultant Medical Geneticist to discuss the findings and their implications.
UAE Regulatory & Data Privacy Adherence
🔒 Data Privacy & Regulatory Compliance: DNA Labs UAE strictly complies with Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) for the handling, storage, and processing of all genetic and personal health data. Our digital health infrastructure meets the stringent requirements of Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. All clinical procedures are governed by Federal Decree-Law No. 4 of 2016 on Medical Liability, ensuring full patient consent and safety rights. Our laboratory management system is ISO 9001:2015 certified (Cert: INT/EGQ/2509DA/3139).
Clinical & Logistical Metadata
| Test Name | Mitochondrial Genome Sequencing |
| Price (AED) | 3,000 |
| Turnaround Time | 21 – 28 Business Days |
| Sample Type / Matrix | Peripheral Whole Blood (VIP Mobile Phlebotomy) |
| Methodology Used | Next-Generation Sequencing (NGS), Sanger Confirmation, and Bioinformatic Curation |
| ICD-10-CM Code | Z13.83 |
| LOINC Code | 94420-9 |
| DHA Facility License & Lab Address | DHA License No: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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