Test Price
2,800 AED✅ Home Collection Available
AARS2 Gene (Combined Oxidative Phosphorylation Deficiency Type 8) DNA Test in UAE | 2,800 AED
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Certified Processing.
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Available daily from 8 AM to 11 PM).
- Clinical Guidance: Complimentary Telephonic Post-Test Clinical Guidance in result interpretation by a DHA-licensed physician.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
This Genetic Test detects pathogenic variants in the AARS2 gene underlying Combined Oxidative Phosphorylation Deficiency Type 8—a rare mitochondrial disorder. Next-Generation Sequencing (NGS) with single-gene resolution provides near-complete coverage of all coding exons and exon-intron boundaries, delivering a diagnostic sensitivity exceeding 99.9%.
| Feature | Our Test | Closest Alternative |
|---|---|---|
| Methodology | Full-gene NGS (single-gene resolution) | Targeted mutation panel / whole-exome |
| Diagnostic Sensitivity | > 99.9% (all coding regions & splice sites) | 85–95% (may miss deep intronic variants) |
| Turnaround Time | 3–4 weeks | 4–8 weeks |
Physician Insight & Safety Protocols
“Dear Patient, this test offers a precise window into your mitochondrial genetics. However, a positive or negative result must be correlated with your full clinical examination and family history by a qualified specialist. Please remember that genetic information empowers management but does not replace the close guidance of your treating physician.”
— Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
Advisory: Medication & Clinical Guidance
Do not discontinue any prescribed medication without consulting your doctor.
Exclusion Criteria
- Individuals without clinical suspicion of mitochondrial disease (inappropriate screening).
- Acute febrile illness or unstable vital signs at the time of blood draw.
- Minors without parental/legal guardian consent as per Federal Decree-Law No. 4 of 2016 on Medical Liability.
Emergency Red Flags – Seek Immediate Medical Attention
- Sudden worsening of neurological symptoms (seizures, loss of consciousness).
- Severe metabolic acidosis (rapid breathing, confusion).
- New-onset cardiac arrhythmia or cardiomyopathy symptoms.
Patient FAQ & Clinical Guidance
1. Why is the AARS2 gene tested for Combined Oxidative Phosphorylation Deficiency?
The AARS2 gene encodes a mitochondrial enzyme critical for energy production; mutations cause Combined Oxidative Phosphorylation Deficiency Type 8, a severe metabolic disorder. NGS sequencing identifies pathogenic variants with near-complete coverage of all coding exons and exon-intron boundaries.
2. How is the sample collected and what is the turnaround time?
A simple blood sample is collected via a virtually painless venipuncture during our VIP home collection visit; the full analytical process delivers results in 3–4 weeks. The dedicated cold-chain logistics maintain sample integrity from your doorstep to our ISO-certified molecular laboratory.
3. Is this test covered by insurance in the UAE?
We offer direct billing verification with all major UAE insurers via WhatsApp at +971 54 548 8731; coverage depends on your policy’s genetic testing clause. Our team will pre-verify eligibility before your appointment to ensure a smooth experience.
UAE Regulatory & Data Privacy Adherence
- All patient data processed in full compliance with Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL).
- Health data protection adheres to Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields.
- Minors’ genetic testing requires parental/legal guardian consent per Federal Decree-Law No. 4 of 2016 on Medical Liability.
- ISO 9001:2015 Certified (Cert: INT/EGQ/2509DA/3139) – Quality Management for Diagnostic Excellence.
Clinical & Logistical Metadata
| Test Name | AARS2 Gene (Combined Oxidative Phosphorylation Deficiency Type 8) DNA Test |
| Price (AED) | 2,800 |
| Turnaround Time | 3–4 weeks |
| Sample Type / Matrix | Peripheral whole blood (3–5 mL in EDTA tube) |
| Methodology Used | Full-gene Next-Generation Sequencing (NGS) with single-gene resolution |
| ICD-10-CM Code | E74.81 |
| LOINC Code | 101638-4 |
| DHA Facility License & Laboratory Address | DHA License No. 1143, Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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