Test Price
2,800 AED✅ Home Collection Available
NDUFS6 Gene (Mitochondrial Complex I Deficiency) Genetic Test in UAE | AED 2800 | 2026 DHA Guidelines
تحليل طفرة جين NDUFS6 لنقص المركب الأول للميتوكوندريا في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Diagnostic Sensitivity: 99.9% via ISO 9001:2015 Certified Processing
حساسية تشخيصية تصل إلى 99.9% عبر معالجة معتمدة وفق معيار ISO 9001:2015
Premium Logistics: Paid Hospital-Grade Home Collection via ISO-Certified Cold-Chain
خدمة السحب المنزلي المدفوعة عبر سلسلة تبريد معتمدة
Clinical Guidance: Telephonic Post-Test Result Interpretation with a DHA-Licensed Specialist
استشارة هاتفية بعد النتيجة مع أخصائي مرخص من هيئة الصحة بدبي
Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731
التحقق المباشر من التأمين عبر واتساب
الفحص معتمد من هيئة الصحة بدبي بموجب المرسوم الاتحادي رقم 41 لسنة 2024 وقانون حماية البيانات الشخصية، ويقدم وفق أحدث إرشادات 2026
Certification: ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139) | Facility License: 9834453
Test Overview & Clinical Comparison
The NDUFS6 Next‑Generation Sequencing test identifies pathogenic variants responsible for mitochondrial complex I deficiency, a severe neurometabolic disorder with variable neurological decline. تحليل جين NDUFS6 بتقنية التسلسل من الجيل التالي يكشف الطفرات المسببة لنقص المركب الأول للميتوكوندريا، وهو اضطراب عصبي استقلابي حاد قد يؤدي إلى اعتلال دماغي مترقٍ. Testing is indicated for symptomatic individuals, at‑risk family members, and for advanced research under strict UAE regulatory oversight.
| Feature | Our Test (NGS) | Closest Alternative (Sanger Sequencing) |
|---|---|---|
| Methodology | Next‑Generation Sequencing (NGS) – Full Gene Coverage | Single‑gene Sanger Sequencing |
| Diagnostic Sensitivity | 99.9% (includes deep intronic & CNV analysis) | ~95% (coding region only) |
| Turnaround Time | 3–4 Weeks | 6–8 Weeks |
| Regulatory Compliance | DHA/MOHAP + ISO 9001:2015, UAE PDPL | Often non‑accredited local labs |
Physician Insight & Clinical Safety Protocol
“As a neurologist, I understand the weight a genetic diagnosis carries for families. This NDUFS6 test provides high‑resolution molecular clarity, but interpretation must always be integrated with clinical examination, MRI findings, and biochemical markers. لا تعتبر النتيجة الجينية وحدها تشخيصًا نهائيًا، بل يجب ربطها بالتقييم السريري الكامل. Please maintain open communication with your multidisciplinary care team.”
— د. برابهاكار ريدي (Dr. Prabhakar Reddy), Consultant Neurologist, DHA License No. 61713011
⚠️ Medication Safety Notice
Do not discontinue prescribed medication or alter treatment based solely on genetic results without consulting your treating physician.
Patient Exclusion Criteria & ER Red Flags
- Exclusion Criteria: This test is not a standalone emergency diagnostic. It must be preceded by a formal genetic counselling session and informed consent. Acute intercurrent illness may delay sample collection for logistical reasons; stable clinical status is preferred.
- Emergency Red Flags: If the patient (infant, child, or adult) develops acute metabolic crisis, refractory seizures, severe lactic acidosis, or unexplained encephalopathy, seek immediate emergency department care — do not wait for genetic results.
Patient FAQ & Clinical Guidance
What is the NDUFS6 gene test, and why is it performed?
Snippet Answer: The NDUFS6 gene test uses next‑generation sequencing to detect mutations causing mitochondrial complex I deficiency, a severe neurological and metabolic condition.
الجواب المقتضب: هو تحليل جيني بتقنية التسلسل المتقدم للكشف عن الطفرات المرتبطة بنقص المركب الأول للميتوكوندريا، وهو اضطراب عصبي استقلابي خطير.
This NGS‑based assay examines the full coding region of the NDUFS6 gene, including exon‑intron boundaries, to identify single nucleotide variants, small insertions/deletions, and copy number changes. It is primarily ordered when clinical features (e.g., Leigh syndrome, leukoencephalopathy) and biochemical evidence point to mitochondrial dysfunction. A pre‑test genetic counselling session is mandatory to construct a three‑generation pedigree and discuss inheritance patterns.
How accurate is this genetic test, and what is the turnaround time?
Snippet Answer: With a diagnostic sensitivity of 99.9% and ISO 9001:2015 certification, results are delivered within 3 to 4 weeks from sample receipt.
الجواب المقتضب: بدقة تصل إلى 99.9% وشهادة ISO 9001:2015، تصدر النتائج خلال 3 إلى 4 أسابيع من استلام العينة.
The high sensitivity is achieved through deep‑coverage NGS and bioinformatic pipelines validated under ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139). Every variant is confirmed by orthogonal methods when necessary. The laboratory adheres to UAE PDPL data privacy standards, and your anonymized data is processed solely for diagnostic purposes. A telephonic post‑test consultation with a DHA‑licensed specialist is provided to help interpret the report.
Do I need a doctor’s referral or genetic counselling before the test?
Snippet Answer: Yes, pre‑test genetic counselling is mandatory to interpret risks, obtain informed consent, and draw a detailed family pedigree chart.
الجواب المقتضب: نعم، الاستشارة الوراثية قبل الفحص إلزامية لتفسير المخاطر، والحصول على الموافقة المستنيرة، ورسم شجرة العائلة التفصيلية.
Under Federal Decree‑Law No. 41 of 2024 on genetic health services, a registered genetic counsellor or clinical geneticist must conduct this session. It can be arranged via our premium tele‑consultation service. The test is not offered to minors without explicit parental consent and in compliance with the UAE Child Data Safeguard Law 2026. Our team will verify referral documentation and insurance eligibility before scheduling home collection.
For booking and insurance verification, contact us via WhatsApp at +971 54 548 8731. Home collection operates daily from 8:00 AM to 11:00 PM. All samples are transported under validated cold-chain protocols.
Prices are inclusive of DHA‑mandated pre‑test counselling and post‑ guidance. This page is reviewed quarterly by our clinical advisory board.
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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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