Test Price
2,800 AED✅ Home Collection Available
MT-CO3 Gene Cytochrome c Oxidase 3 Deficiency Genetic Test in UAE | 2800 AED | DHA Licensed
Executive Summary & Core Metrics
Executive Summary
This DHA-licensed genetic test delivers 99.9% diagnostic sensitivity via ISO-accredited next-generation sequencing (NGS) for cytochrome c oxidase 3 deficiency. Premium logistics include VIP mobile phlebotomy and temperature-controlled cold-chain home collection. Post-test clinical guidance is provided by a board-certified genetic specialist. Direct billing validation is available via WhatsApp at +971 54 548 8731.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing.
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection and VIP Mobile Phlebotomy.
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
MT-CO3 Gene Cytochrome c Oxidase 3 Deficiency Genetic Test uses next-generation sequencing (NGS) to analyze the entire mitochondrial MT-CO3 gene for pathogenic variants causing complex IV deficiency. This disorder is linked to severe neurological and mitochondrial syndromes. The test delivers comprehensive coverage of coding regions and splice sites.
| Feature | Our Test (Premium) | Closest Alternative |
|---|---|---|
| Precision | NGS full gene sequencing | Sanger sequencing (limited targets) |
| Method | Illumina® NGS Platform | PCR-based targeted panels |
| Speed (TAT) | 3–4 Weeks | 4–8 Weeks |
Physician Insight & Safety Protocols
“While this NGS test offers high diagnostic accuracy, results must be correlated with clinical history and neurological evaluation. I advise patients not to discontinue any prescribed medication without consulting their treating neurologist. Our team is here to guide you through result interpretation.”
Medication Advisory
⚠️ Medication Warning
Do not discontinue prescribed medication without consulting your doctor. This test is a diagnostic aid and does not replace medical advice.
Exclusion Criteria & ER Red Flags
- Exclusion: Patients with active bleeding disorders, severe thrombocytopenia, or inability to provide a blood sample should consult the ordering physician before booking.
- Emergency Red Flags: If you experience sudden seizures, loss of consciousness, stroke-like episodes, or severe metabolic crisis, seek emergency medical attention immediately — this test is not for acute diagnostics.
Patient FAQ & Clinical Guidance
1. What is the MT-CO3 genetic test and who should consider it?
This NGS test sequences the entire MT-CO3 gene to identify pathogenic variants linked to mitochondrial cytochrome c oxidase deficiency disorders. It is recommended for individuals with unexplained neurological symptoms, family history of mitochondrial disease, or those seeking genetic confirmation under physician guidance.
2. What sample is required and how is collection done?
Blood on FTA card, whole blood, or extracted DNA enables precise NGS analysis of MT-CO3. Our VIP mobile phlebotomy team collects a finger-prick drop or venous sample at your home, office, or hospital, ensuring cold-chain transport.
3. How long do results take and how will I receive them?
Results are typically available within 3 to 4 weeks from sample receipt at the lab. Reports are delivered securely via encrypted PDF, with optional telephonic clinical guidance from our DHA-licensed specialist.
UAE Regulatory & Data Privacy Adherence
Compliance Framework
This test 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. Clinical safety and patient consent follow Federal Decree-Law No. 4 of 2016 on Medical Liability. All data is encrypted, stored within the UAE, and handled under DHA oversight.
Clinical & Logistical Metadata
| Test Name | MT-CO3 Gene Cytochrome c Oxidase 3 Deficiency Genetic Test (NGS) |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3–4 Weeks |
| Sample Type / Matrix | Whole Blood, Dried Blood Spot (FTA card), or Extracted DNA |
| Methodology Used | Next-Generation Sequencing (Illumina® Platform) |
| ICD-10-CM Code | E88.49 |
| LOINC Code | 87600-5 |
| DHA Facility License & Laboratory Address | License No. 1143 – Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
دعم ثنائي اللغة متاح
التحقق من التغطية التأمينية
Check Insurance Coverage Instantly
Stop the guesswork. Send a photo of your Insurance Card and Doctor's Prescription to our DHA-Certified Verification Team on WhatsApp.
توقف عن التخمين. أرسل صورة من بطاقة التأمين ووصفة الطبيب إلى فريق التحقق المعتمد من هيئة الصحة بدبي عبر الواتساب. احصل على تحديث الحالة في دقائق.
Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians