Test Price
2,800 AED✅ Home Collection Available
UQCC2 Gene (Mitochondrial Complex III Deficiency, Nuclear Type 7) Genetic Test in UAE – 2,800 AED – DHA Licensed
Executive Summary & Core Metrics
Accuracy Guarantee
99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited NGS Processing with Sanger confirmation for all pathogenic variants.
Premium Logistics
VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection – Available daily from 8 AM to 11 PM across all UAE emirates by DHA-licensed phlebotomists.
Clinical Guidance
Post-test telephonic clinical interpretation and genetic counselling support provided by a Consultant Medical Geneticist.
Insurance Support
Direct Billing Verification via WhatsApp +971 54 548 8731. All genetic data handled under Federal Decree-Law No. 45 of 2021 (PDPL).
Test Overview & Methodology
The UQCC2 gene next‑generation sequencing test definitively identifies pathogenic variants causing mitochondrial complex III deficiency, nuclear type 7—a severe metabolic disorder. In the UAE, this 2,800 AED test provides a 3–4 week turnaround time using ISO‑certified NGS with Sanger confirmation, essential for accurate diagnosis, carrier screening, and family planning. Targeted analysis covers the entire coding region and splice sites of the UQCC2 gene.
| Feature | Our UQCC2 NGS Test | Closest Alternative (Muscle Biopsy Enzyme Assay) |
|---|---|---|
| Methodology | Next‑Generation Sequencing (NGS) with Sanger confirmation | Spectrophotometric enzyme activity in muscle tissue |
| Diagnostic Sensitivity | >99.9% for targeted nuclear variants | ~85-90% for complex III deficiency |
| Turnaround Time | 3–4 Weeks | 6–8 Weeks |
| Sample Type | Whole blood, extracted DNA, or FTA card | Invasive muscle biopsy |
| UAE Compliance | DHA/MOHAP-licensed laboratory, ISO 9001:2015 | Variable, often sent abroad |
Physician Insight & Safety Protocols
“As a medical geneticist, I recognize that a suspected mitochondrial disorder can be deeply concerning. This NGS test provides a definitive molecular diagnosis, but results must always be interpreted alongside clinical and biochemical assessments. Please consult your physician before making any changes to medications or supplements.”
— Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
Medication Advisory
Do not discontinue or adjust any prescribed medication, including mitochondrial supplements or “mitochondrial cocktails,” without consulting your treating physician. Genetic results alone should not drive immediate therapeutic changes. Always correlate with clinical and biochemical findings.
Exclusion Criteria & Emergency Red Flags
- Exclusion: Patients who have received an allogeneic blood transfusion or bone marrow transplant within the last 3 months (donor DNA may confound results).
- Exclusion: Inability to provide informed consent or absence of legal guardian for minors (in compliance with Federal Decree-Law No. 4 of 2016 on Medical Liability).
- Emergency Red Flag: If the patient develops acute metabolic crisis—such as severe lactic acidosis, refractory hypoglycemia, seizures, or encephalopathy—seek immediate medical care at the nearest emergency department before scheduling elective genetic testing.
Patient FAQ & Clinical Guidance
1. What is the UQCC2 gene test and why is it done?
The UQCC2 NGS test detects pathogenic variants in the UQCC2 gene associated with mitochondrial complex III deficiency, nuclear type 7, aiding diagnosis and family planning. It is indicated for individuals with clinical symptoms such as muscle weakness, developmental delay, elevated lactate, or a family history of mitochondrial disease. Genetic counselling is mandatory before testing and is provided as part of the service.
2. How is the sample collected and how long for results?
A simple blood draw or FTA card sample is collected by a DHA-licensed phlebotomist at your home, with results in 3–4 weeks. We offer a VIP mobile phlebotomy service across the UAE from 8 AM to 11 PM daily. The sample is transported in a temperature-controlled, ISO-certified cold chain to our DHA-licensed genomic laboratory. DNA extraction and NGS sequencing are performed; the final report is reviewed by a Consultant Medical Geneticist before release.
3. Is the test covered by UAE health insurance?
Many UAE insurers cover genetic testing when medically necessary. Our team verifies your coverage via WhatsApp at +971 54 548 8731. We assist with prior authorization and direct billing with major insurers such as Daman, AXA, Sukoon, and Neuron. All genetic data is handled under Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) and used solely for diagnostic purposes.
UAE Regulatory & Data Privacy Adherence
Data Privacy: All genetic and personal data are 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.
Medical Liability: Patient consent and clinical safety protocols follow Federal Decree-Law No. 4 of 2016 on Medical Liability.
Laboratory Licensing: This test is performed at DNA Labs UAE, DHA Facility License Number 1143, located at Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE.
Clinical & Logistical Metadata
| Test Name | UQCC2 Gene (Mitochondrial Complex III Deficiency, Nuclear Type 7) Genetic Test – NGS |
| Price (AED) | 2,800 |
| Turnaround Time | 3–4 Weeks |
| Sample Type / Matrix | Whole blood, extracted DNA, or FTA card |
| Methodology Used | Next-Generation Sequencing (NGS) with Sanger confirmation |
| ICD-10-CM Code | E88.40, G71.3, Z13.79 |
| LOINC Code | 48776-7 |
| DHA Facility License & Address | License 1143 – Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE – 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