Test Price
2,800 AED✅ Home Collection Available
TTC19 Gene Mitochondrial Complex III Deficiency, Nuclear Type 2 Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين TTC19 المرتبط بنقص المركب الثالث في الميتوكوندريا من النوع النووي الثاني في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 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.
الملخص التنفيذي
- ضمان الدقة: حساسية تشخيصية بنسبة 99.9% وفق معايير ISO 9001:2015.
- الخدمات اللوجستية المتميزة: جمع عينات منزلي على مستوى المستشفيات عبر سلسلة تبريد معتمدة من ISO وخدمة سحب الدم المتنقلة VIP.
- الإرشاد السريري: إرشاد هاتفي بعد الاختبار لتفسير النتائج.
- التأمين: التحقق المباشر من التغطية التأمينية عبر واتساب +971 54 548 8731.
Overview
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. (باختصار: يكشف تحليل جين TTC19 عن الطفرات المسؤولة عن نقص المركب الثالث في الميتوكوندريا والذي يسبب اضطرابات عصبية حادة).
| 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 | 3–4 Weeks | 4–6 Weeks |
Physician Insight & Safety Protocol
“As a DHA-licensed neurologist, I emphasize that genetic testing for TTC19 is a critical step in confirming mitochondrial complex III deficiency, but it must be integrated with clinical phenotype, neuroimaging, and family history. Results guide precision management and inform reproductive options, yet never replace holistic clinical judgment.”
— Dr. PRABHAKAR REDDY, DHA License: 61713011
Medication Warning
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 legal guardian and explicit genetic counselling as per UAE CDS Law 2026.
- 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.
Pre-Test Requirements
- Provide a detailed clinical history highlighting neurological symptoms, mitochondrial disease suspicion.
- Mandatory genetic counselling session to draw a pedigree chart of family members affected by TTC19-related mitochondrial complex III deficiency.
- Most common sample: 2–3 mL whole blood in EDTA tube, or extracted DNA (1 µg), or one drop of blood on FTA card.
- Avoid dietary supplements like CoQ10 or idebenone for 48 hours prior, as they may interfere with functional studies (note: not directly for DNA test but advised).
Patient FAQ & Clinical Guidance
1. What does TTC19 Genetic Testing detect, and how long does it take in the UAE?
Direct answer: This test identifies pathogenic mutations in the TTC19 gene causing mitochondrial complex III deficiency, nuclear type 2, using high-throughput NGS with results in 3–4 weeks. (يكشف هذا الاختبار عن الطفرات المرضية في جين TTC19 المسببة لنقص المركب الثالث في الميتوكوندريا النمط النووي الثاني، ويعطي النتائج في غضون 3-4 أسابيع).
2. How is the sample collected, and are home services available for neurological patients?
Direct answer: 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. (يقوم فني سحب دم مدرب بجمع العينة عبر خدمتنا المتنقلة VIP في جميع إمارات الدولة، مع ضمان سلسلة تبريد مثالية وراحة للمرضى المصابين بأمراض عصبية).
3. Is this covered by UAE health insurance, and how can I verify?
Direct answer: 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. (تتوفر تغطية تأمينية مباشرة مع كبرى شركات التأمين مثل ضمان وأكسا؛ أرسل واتساب إلى +971 54 548 8731 مع بطاقة الهوية الإماراتية ورقم الوثيقة للتحقق الفوري).
UAE Regulatory & Quality Compliance
- Licensed facility under DHA/MOHAP License No. 9834453.
- Accredited ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139) for laboratory quality management.
- Testing adheres to Federal Decree-Law No. 41 of 2024 (Art. 87) on genetic privacy, and UAE Personal Data Protection Law (PDPL).
- For minors, compliance with CDS Law 2026 requiring parental consent and genetic counselling.
دعم ثنائي اللغة متاح
التحقق من التغطية التأمينية
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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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