Test Price
2,800 AEDโ Home Collection Available
TTC19 Gene Mitochondrial Complex III Deficiency, Nuclear Type 2 Genetic Test in UAE | 2800 AED | DHA Guidelines
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing.
- Premium Logistics: Hospital-Grade Home Collection via ISO Certified Cold-Chain and VIP Mobile Phlebotomy (available daily 8 AM โ 11 PM).
- Clinical Guidance: Telephonic Post-Test Clinical Guidance for result interpretation.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The TTC19 gene analysis detects pathogenic mutations causing mitochondrial complex III deficiency, a severe neurological disorder. This next-generation sequencing (NGS) test provides definitive diagnosis for affected individuals and carrier status for family members. Our accredited laboratory utilizes Illumina-based sequencing for full gene coverage with 99.9% diagnostic sensitivity.
| Feature | Our Test (NGS) | Closest Alternative (Sanger Sequencing) |
|---|---|---|
| Precision | 99.9% diagnostic sensitivity, full gene coverage | ~95%, limited to known mutations |
| Method | Next-Generation Sequencing (Illumina) | Sanger Sequencing |
| Turnaround Time | 3โ4 Weeks | 4โ6 Weeks |
Pre-Test Requirements
- Provide a detailed clinical history highlighting neurological symptoms and mitochondrial disease suspicion.
- Mandatory genetic counselling session to construct a pedigree chart of family members affected by TTC19-related mitochondrial complex III deficiency.
- Most common sample: 2โ3 mL whole blood in EDTA tube, or extracted DNA (1 ยตg), or one drop of blood on FTA card.
- Avoid dietary supplements like CoQ10 or idebenone for 48 hours prior (advised for functional consistency).
Physician Insight & Safety Protocols
โAs a DHA-licensed Consultant Medical Geneticist, I emphasize that TTC19 genetic testing is critical for confirming mitochondrial complex III deficiency. Results must be integrated with clinical phenotype, neuroimaging, and family history. They guide precision management and inform reproductive options, yet never replace holistic clinical judgment.โ
โ Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
Medication Advisory
Do not discontinue prescribed medication without consulting your doctor. Genetic test results do not substitute for ongoing medical management.
Safety Exclusions & Red Flags
- This test is contraindicated for minors unless accompanied by a legal guardian and explicit genetic counselling as per Federal Decree-Law No. 4 of 2016 on Medical Liability.
- Do not proceed if the patient is acutely unstable or requires immediate life-saving interventions.
- If you experience sudden neurological deterioration (e.g., seizures, loss of consciousness, respiratory distress), seek emergency care immediately.
- For patients on anticoagulant therapy, home phlebotomy is performed under strict safety protocols; inform the team beforehand.
Patient FAQ & Clinical Guidance
1. What does TTC19 Genetic Testing detect, and how long does it take in the UAE?
This test identifies pathogenic mutations in the TTC19 gene causing mitochondrial complex III deficiency, nuclear type 2, using high-throughput NGS with results in 3โ4 weeks.
2. How is the sample collected, and are home services available for neurological patients?
A trained phlebotomist collects blood via our VIP mobile service across all UAE emirates, ensuring cold-chain integrity and minimal stress for neuro-affected individuals. Home collection is available daily from 8 AM to 11 PM.
3. Is this test covered by UAE health insurance, and how can I verify coverage?
Direct billing with major insurers (Daman, AXA, etc.) is available. WhatsApp +971 54 548 8731 with your Emirates ID and policy number for instant verification.
UAE Regulatory & Data Privacy Adherence
- Licensed facility under DHA Facility License Number: 1143.
- Accredited ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139) for laboratory quality management.
- All testing adheres to 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.
- Clinical safety and patient consent are governed by Federal Decree-Law No. 4 of 2016 on Medical Liability.
Clinical & Logistical Metadata
| Test Name | TTC19 Gene Mitochondrial Complex III Deficiency, Nuclear Type 2 Genetic Test |
| Price (AED) | 2800 |
| Turnaround Time | 3โ4 Weeks |
| Sample Type / Matrix | Peripheral Whole Blood (2-3 mL EDTA) โ VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection |
| Methodology Used | Next-Generation Sequencing (Illumina) |
| ICD-10-CM Code | E88.49 (Other mitochondrial metabolism disorders) |
| LOINC Code | 83573-1 |
| DHA Facility License & Address | License No: 1143 | DNA Labs UAE โ Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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