Test Price
2,800 AEDโ Home Collection Available
MPV17 Gene Mitochondrial DNA Depletion Syndrome Type 6 Genetic Test in UAE | 2,800 AED | DHA Licensed Laboratory
Executive Summary & Core Metrics
Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing.
Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (8 AM โ 11 PM daily).
Clinical Guidance: Complimentary Telephonic Post-Test Genetic Counseling by a DHA-Licensed Consultant Medical Geneticist.
Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The MPV17 Gene Genetic Test offers unmatched precision and rapid turnaround compared to traditional single-gene Sanger sequencing. It uses Next-Generation Sequencing (NGS) to detect pathogenic variants in the MPV17 gene associated with Mitochondrial DNA Depletion Syndrome Type 6, a hepatocerebral disorder.
| Feature | Our Test (NGS) | Closest Alternative (Single-Gene Sanger) |
|---|---|---|
| Methodology | Next-Generation Sequencing (NGS) with full gene coverage | Sanger sequencing, limited to known hotspots |
| Diagnostic Sensitivity | 99.9% for all variant types (SNVs, indels, CNVs) | ~95%, may miss large rearrangements |
| Turnaround Time | 3โ4 Weeks | 6โ8 Weeks |
| Regulatory Compliance | DHA & MOHAP Approved, ISO 9001:2015 Certified | May not meet UAE laboratory standards |
Physician Insight & Safety Protocols
โAs a Consultant Medical Genetics, I emphasize that genetic results must be interpreted alongside the full clinical presentation and family history of the patient. This NGS-based MPV17 test provides a definitive molecular diagnosis but does not replace ongoing clinical management. Always discuss therapy adjustments with your primary physician.โ โ Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403.
Do not discontinue prescribed medication or alter treatment without consulting your doctor.
Safety Exclusion Criteria & ER Red Flags
- Exclusion: Severe acute illness, known coagulopathy without medical clearance, inability to provide informed consent.
- ER Red Flags: Sudden onset of seizures, severe lethargy or loss of consciousness, acute liver dysfunction (jaundice, vomiting, bleeding). If experienced, seek emergency care immediately.
Patient FAQ & Clinical Guidance
1. What is the purpose of MPV17 gene testing?
This NGS test identifies pathogenic variants in the MPV17 gene causing mitochondrial DNA depletion syndrome type 6, enabling accurate diagnosis and targeted management. It is recommended for individuals with hepatocerebral symptoms, unexplained lactic acidosis, or a family history of the disorder. Early identification guides treatment and surveillance strategies.
2. How is the test performed?
A peripheral blood sample or DNA FTA card is collected by a DHA-licensed phlebotomist via our VIP Mobile Phlebotomy service. The sample is transported under temperature-controlled cold-chain conditions to our ISO-certified laboratory. Genetic counseling is provided before collection to review family history and obtain informed consent.
3. What do positive results mean?
A positive result confirms the genetic diagnosis of mitochondrial DNA depletion syndrome type 6, facilitating prognosis, family planning, and interdisciplinary follow-up with a neurologist and gastroenterologist. The report includes variant interpretation and recurrence risk assessment.
UAE Regulatory & Data Privacy Adherence
Data Privacy & Security: Your genetic data is processed in full compliance with 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 adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability.
Accreditation: ISO 9001:2015 Certified Laboratory (Cert: INT/EGQ/2509DA/3139). DHA Facility License: 1143. Corporate Lab: DNA Labs UAE.
Clinical & Logistical Metadata
| Test Name | MPV17 Gene Mitochondrial DNA Depletion Syndrome Type 6 Genetic Test |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3โ4 Weeks |
| Sample Type / Matrix | Peripheral Blood or DNA FTA Card (VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection Available daily 8 AM โ 11 PM) |
| Methodology Used | Next-Generation Sequencing (NGS) with Full Gene Coverage |
| ICD-10-CM Code | E88.49 |
| LOINC Code | 82939-0 |
| DHA Facility License & Laboratory Address | DHA License: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | Corporate Lab: DNA Labs UAE |
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ISMS 27001:2022
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All reports reviewed by DHA-Certified physicians