Test Price
3,000 AED✅ Home Collection Available
NGSMito Comprehensive Genetic Test in UAE | 3,000 AED | DHA Licensed
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Available daily from 8 AM to 11 PM).
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation by DHA-licensed specialists.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The NGSMito Comprehensive Genetic Test utilizes next‑generation sequencing to analyze the entire mitochondrial genome, identifying pathogenic variants linked to neurological and multisystem mitochondrial disorders. This high‑resolution test supports accurate diagnosis, prognosis, and personalized management for conditions such as mitochondrial encephalopathy, myopathy, and progressive external ophthalmoplegia.
| Feature | Our Test (NGSMito Comprehensive) | Closest Alternative (Single‑Gene Sequencing) |
|---|---|---|
| Precision | Full mtDNA coverage, detects point mutations, deletions, depletion | Limited to one or few genes, may miss complex variants |
| Methodology | Next‑Generation Sequencing (NGS) with bioinformatic analysis | Sanger sequencing or targeted PCR |
| Turnaround Time | 3–4 Weeks | 6–8 Weeks (when multiple single‑gene tests are ordered) |
Physician Insight & Safety Protocols
"As a consultant in medical genetics, I recognize the diagnostic complexity of mitochondrial disorders. This comprehensive NGS test offers deep insight into the mitochondrial genome, helping to uncover pathogenic variants that may explain a range of clinical presentations. However, genetic results must always be interpreted within the full clinical context. Continue all prescribed medications and consult your treating physician before acting on the findings."
⚠️ Do not discontinue prescribed medication without consulting your doctor.
Exclusion Criteria & Emergency Red Flags
- Acute neurological crisis (e.g., stroke‑like episodes, seizures, sudden vision loss) – seek emergency care before scheduling this elective test.
- Unstable clinical condition requiring intensive monitoring or immediate therapeutic intervention.
- Known diagnosis already confirmed by a validated laboratory; a genetic counsellor can advise if retesting is beneficial.
- If you experience severe muscle weakness, respiratory difficulty, or loss of consciousness, go to the nearest emergency department.
Patient FAQ & Clinical Guidance
1. What does the NGSMito Comprehensive Genetic Test detect, and how accurate is it?
The test detects point mutations, large deletions, and mtDNA depletion across the entire mitochondrial genome with over 99.9% diagnostic sensitivity. This includes pathogenic variants responsible for mitochondrial myopathy (G71.3), mitochondrial metabolism disorders (E88.40), and progressive external ophthalmoplegia (H49.81).
2. How is the sample collected and what preparation is required?
Our VIP mobile phlebotomy team collects a small amount of whole blood, extracted DNA, or a dried blood spot on an FTA card at your home, strictly following cold-chain protocols. A pre-test genetic counselling session is mandatory to draw a pedigree and discuss the implications of mitochondrial inheritance.
3. How will I receive my results and what support is provided?
Results are available in 3 to 4 weeks via a secure encrypted report; a DHA-licensed geneticist will provide a telephonic post-test clinical guidance session to explain the findings and recommend next steps. Insurance direct billing verification is handled instantly through WhatsApp +971 54 548 8731.
UAE Regulatory & Data Privacy Adherence
This service adheres to 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 samples are processed in an ISO 9001:2015 certified facility (Cert: INT/EGQ/2509DA/3139; DHA Facility License: 1143) under DHA-recognized clinical standards. Your health information is encrypted and never shared without explicit consent.
Clinical & Logistical Metadata
| Test Name | NGSMito Comprehensive Genetic Test |
| Price (AED) | 3,000 |
| Turnaround Time | 3–4 Weeks |
| Sample Type / Matrix | Whole Blood, Extracted DNA, or Dried Blood Spot (FTA card) |
| Methodology Used | Next-Generation Sequencing (NGS) with Bioinformatic Analysis |
| ICD-10-CM Code | G71.3, E88.40, H49.81 |
| LOINC Code | 101383-9 |
| DHA Facility License & Laboratory Address | DHA License No: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, 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