Test Price
2,800 AED✅ Home Collection Available
UQCRB Gene – Mitochondrial Complex III Deficiency Genetic Test in UAE | 2800 AED | DHA Licensed
Executive Summary & Core Metrics
Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing.
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Available daily from 8 AM to 11 PM).
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The UQCRB Gene – Mitochondrial Complex III Deficiency Genetic Test is a high‑precision genetic test that analyzes the UQCRB gene for pathogenic variants linked to mitochondrial complex III deficiency, a rare neurological disorder. This next‑generation sequencing (NGS) assay offers comprehensive coverage of coding regions and splice sites, ensuring >99.9% diagnostic sensitivity and specificity in detecting causative mutations.
| Feature | Our UQCRB Focused NGS Test | Closest Alternative (Mitochondrial Panel NGS) |
|---|---|---|
| Precision | 99.9% sensitivity for UQCRB variants with 500× mean coverage | ~95% sensitivity per gene due to lower coverage (200×) |
| Method | Full gene NGS (Illumina® platform) with Sanger confirmation | Multi‑gene panel NGS; may miss deep intronic variants |
| Turnaround Time | 3–4 weeks guaranteed | 4–6 weeks typical |
Physician Insight & Safety Protocols
“As your Consultant Medical Geneticist, I emphasize that genetic test results must always be correlated with clinical findings and family history. This test identifies DNA variants; a positive result does not constitute a diagnosis on its own. Comprehensive post-test genetic counseling is essential for understanding implications and management.”
— Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
Advisory
Genetic results should be interpreted by a qualified geneticist. Do not make medical decisions based solely on this test. Always consult your healthcare provider before starting or stopping any treatment.
Exclusion Criteria & Emergency Red Flags
- Exclusion Criteria: Inability to provide a blood or DNA sample; lack of clinical suspicion for a mitochondrial disorder; patient under 18 years without documented parental consent.
- ER Red Flags: If you experience sudden vision loss, severe muscle weakness, seizures, or signs of lactic acidosis (rapid breathing, confusion), seek emergency medical attention immediately.
Patient FAQ & Clinical Guidance
1. What is the UQCRB gene test?
This test detects DNA mutations in the UQCRB gene responsible for mitochondrial complex III deficiency. It examines the full coding sequence to identify pathogenic variants that impair complex III of the mitochondrial respiratory chain, helping confirm a clinical diagnosis or guide further neurological evaluation.
2. How is the sample collected?
A simple blood draw is all that’s required. Our ISO‑certified VIP mobile phlebotomy service ensures proper cold‑chain handling, and a trained phlebotomist can visit you between 8 AM and 11 PM for maximum convenience.
3. What does a positive result mean for my health?
A positive result indicates a disease‑causing variant in UQCRB, increasing the risk of mitochondrial complex III deficiency. It does not automatically mean you will develop symptoms; the result must be correlated with clinical findings by a neurologist, and genetic counseling is recommended to discuss implications for family members.
UAE Regulatory & Data Privacy Adherence
Compliance & Data Protection
This service strictly adheres to the 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. Our genomics laboratory holds ISO 9001:2015 certification (Cert: INT/EGQ/2509DA/3139), ensuring the highest quality management standards. All patient data is handled in compliance with DHA regulations.
Clinical & Logistical Metadata
| Test Name | UQCRB Gene – Mitochondrial Complex III Deficiency Genetic Test |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3–4 weeks |
| Sample Type / Matrix | Peripheral Whole Blood (3–5 mL in EDTA tube) |
| Methodology Used | Next-Generation Sequencing (NGS) with Sanger Confirmation |
| ICD-10-CM Code | E88.49 |
| LOINC Code | 72296-1 |
| 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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Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians