Test Price
2,800 AED✅ Home Collection Available
COQ9 Gene Coenzyme Q10 Deficiency Type 5 Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين COQ9 لنقص الإنزيم المساعد Q10 النوع الخامس في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary – ملخص تنفيذي
فحص وراثي دقيق لتشخيص نقص الإنزيم المساعد Q10 النوع الخامس، معتمد من هيئة الصحة بدبي وبموجب القانون الاتحادي رقم 41 لسنة 2024.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139) accredited NGS processing.
- Premium Logistics: Paid Hospital‑Grade Home Collection via ISO‑Certified Cold‑Chain logistics, available daily 8 AM – 11 PM.
- Clinical Guidance: Complimentary telephonic post‑test clinical interpretation session with a DHA‑licensed neurologist.
- Insurance: Direct Billing Verification via WhatsApp: +971 54 548 8731.
Overview
This next‑generation sequencing test analyses the entire coding region of the COQ9 gene to confirm primary coenzyme Q10 deficiency type 5, an autosomal recessive mitochondrial disorder often presenting with infantile‑onset encephalopathy, seizures, and ataxia. يُستخدم هذا التحليل الجيني لتأكيد الطفرات المسببة للمرض وتوجيه العلاج البديل بالإنزيم المساعد Q10.
| Feature | Our Test | Closest Alternative |
|---|---|---|
| Precision | Full‑gene NGS with Sanger confirmation | Targeted mutation panel only |
| Method | Illumina NovaSeq X Plus, ISO 9001:2015 | Sanger sequencing (limited resolution) |
| Turnaround Time | 3–4 Weeks | 6–8 Weeks |
Physician Insight & Safety Protocol
Dr. Prabhakar Reddy, DHA: 61713011
“As a neurologist, I emphasise that a genetic result alone does not define a patient’s future; clinical correlation with symptoms, biochemical markers, and family history is essential. This test provides a molecular foundation for a tailored therapeutic approach, but it must always be interpreted within the broader clinical context. I encourage every patient to discuss their results with a multidisciplinary team including a genetic counsellor and metabolic specialist.”
⚠ Medication Warning
Do not discontinue any prescribed medication or start Coenzyme Q10 supplementation without consulting your doctor. Abrupt changes may provoke metabolic decompensation.
Safety Exclusion Criteria & Emergency Red Flags
- Exclusion: Newborns under 28 days with severe metabolic instability require prior hospital‑based stabilisation before sample collection.
- Red Flag: If the patient develops acute encephalopathy, refractory seizures, or severe lactic acidosis within the waiting period, seek emergency medical care immediately.
- Contraindication: This test cannot rule out all forms of CoQ10 deficiency; negative results do not exclude other mitochondrial disorders.
Patient FAQ & Clinical Guidance
How long does the COQ9 NGS test take and what does the price include?
The test reports within 3 to 4 weeks, inclusive of genetic counselling, home blood collection, and a tele‑health interpretation session.
The 2800 AED fee covers sample transport, ISO‑certified NGS analysis, Sanger confirmation, and a detailed clinical report.
ما هي العينة المطلوبة لاختبار جين COQ9؟
يمكن جمع العينة من الدم الكامل أو الحمض النووي المستخلص أو بقعة دم جافة على بطاقة FTA.
A single venous blood draw (3‑5 mL in EDTA tube) or a dried blood spot card is sufficient; our phlebotomist can perform the collection at your home.
Is this covered by UAE health insurance?
Yes, many UAE insurance plans cover genetic testing for suspected mitochondrial disorders when pre‑authorised. Use our WhatsApp (+971 54 548 8731) for direct billing verification before booking.
Facility License: 9834453 | ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139) | DHA Compliant | Federal Decree‑Law No. 41 of 2024 (Art. 87) | UAE PDPL Data Privacy
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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.
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All reports reviewed by DHA-Certified physicians