Test Price
2,800 AED✅ Home Collection Available
NDUFV2 Gene Mitochondrial Complex I Deficiency Genetic Test in UAE | 2800 AED | DHA Licensed
Executive Summary & Core Metrics
✅ Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited NGS Processing.
✅ Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Daily 8 AM – 11 PM).
✅ Clinical Guidance: Telephonic Post-Test Clinical Genetic Counseling by Dr. Lina Quteineh’s team.
✅ Insurance & Billing: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The NDUFV2 gene NGS test screens for mutations causing mitochondrial complex I deficiency, a severe neurometabolic disorder often presenting as Leigh syndrome. This test helps neurologists, geneticists, and pediatricians confirm a diagnosis, guide treatment, and inform family planning.
| Feature | Our NDUFV2 NGS Test | Whole Exome Sequencing |
|---|---|---|
| Precision | Targeted high-depth coverage ≥500x for NDUFV2 | Variable depth, may miss low-level variants |
| Method | Next Generation Sequencing (NGS) – Gene Panel | NGS – Whole Exome |
| Speed | 3–4 Weeks | 6–8 Weeks+ |
| Cost | 2,800 AED | 5,000 – 8,000 AED |
Physician Insight & Safety Protocols
“As a Consultant Medical Geneticist, I emphasize that NDUFV2 variant interpretation requires careful segregation analysis within the family pedigree. A positive result provides a molecular diagnosis, but phenotypic severity can vary widely. Genetic counseling is mandatory before and after testing. Never adjust metabolic therapies without consulting the managing specialist.”
— Lina Osama Zaki Quteineh | Consultant Medical Genetics | DHA Registration ID: 9294403
Advisory & Safety Notice
Medication & Metabolic Therapy Warning
Patients undergoing evaluation for mitochondrial disorders must not discontinue prescribed metabolic cocktails, vitamins, or seizure medications without explicit consultation with their managing neurologist or metabolic specialist.
Exclusion Criteria & Emergency Red Flags
- Exclusion: Recent blood transfusion within 2 weeks; uncontrolled bleeding disorders or anticoagulant therapy incompatible with venipuncture.
- ER Red Flags: If the patient develops acute metabolic crisis (intractable vomiting, extreme lethargy, seizures, or loss of consciousness), seek emergency medical care immediately — do not wait for test results.
Patient FAQ & Clinical Guidance
1. What is the accuracy of the NDUFV2 genetic test?
With Next-Generation Sequencing and rigorous bioinformatics analysis, our test achieves 99.9% analytical sensitivity for detecting known pathogenic variants in the NDUFV2 gene.
2. How is the sample collected at home?
Our DHA-licensed phlebotomists collect a small blood sample via venipuncture or a finger-prick spot on an FTA card, ensuring cold-chain transport back to the laboratory for analysis.
3. How long does it take to get results and what do they mean?
Results are available within 3–4 weeks. The report includes a detailed interpretation by a consultant medical geneticist, outlining the specific variant detected and its clinical significance.
UAE Regulatory & Data Privacy Adherence
This test is performed under the regulatory oversight of the Dubai Health Authority (DHA) and the UAE Ministry of Health, adhering to the highest standards of data privacy and security. We comply fully with 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. All clinical procedures and patient consent protocols are governed by Federal Decree-Law No. 4 of 2016 on Medical Liability. Your genetic data is encrypted, confidential, and used solely for diagnostic purposes.
Clinical & Logistical Metadata
| Test Name | NDUFV2 Gene Mitochondrial Complex I Deficiency Genetic Test (NGS) |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3 – 4 Weeks |
| Sample Type / Matrix | Whole Blood (EDTA) or Dried Blood Spot (FTA Card) |
| Methodology Used | Next Generation Sequencing (NGS) – Targeted Gene Panel |
| ICD-10-CM Code | E88.49 (Mitochondrial metabolism disorder, unspecified) |
| LOINC Code | 82173-6 (Gene panel NGS test) |
| DHA Facility License & Address | License No: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | Corporate Lab: 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