Test Price
2,500 AED✅ Home Collection Available
MERRF Mutation Detection Test in UAE | 2500 AED | DHA Licensed
Executive Summary & Core Metrics
- ✓ Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited PCR Amplification.
- ✓ Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Daily 8 AM – 11 PM).
- ✓ Clinical Guidance: Telephonic Post-Test Genetic Interpretation by DHA-Licensed Consultant Medical Geneticist.
- ✓ Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The MERRF Mutation Detection Test is a targeted polymerase chain reaction (PCR) based analysis that identifies pathogenic variants in the mitochondrial DNA associated with myoclonic epilepsy with ragged red fibres syndrome. This confirms a clinical suspicion of mitochondrial encephalomyopathy and guides treatment planning.
| Feature | Our MERRF Test | Closest Alternative |
|---|---|---|
| Precision | Targeted MERRF gene PCR sequencing | Whole mitochondrial genome NGS |
| Method | PCR Amplification + Sanger validation | Next-Generation Sequencing |
| Turnaround | 10 working days | 14–21 working days |
| Price (AED) | 2500 | ~5000+ |
Physician Insight & Safety Protocols
“MERRF mutation results must be interpreted alongside neurological history, EEG, and metabolic assays. A negative finding does not rule out other mitochondrial disorders, and every positive result should prompt comprehensive genetic counselling. Clinical correlation is essential.”
— Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
Advisory: Medication Continuity
Do not discontinue prescribed anti-epileptic medication without consulting your doctor. Abrupt withdrawal may trigger severe seizures or status epilepticus.
Exclusion Criteria & Red Flags
- Exclusion: Hemolyzed, clotted, or frozen blood sample; missing mandatory Genomics Clinical Information Requisition Form (Form 20); incorrect anticoagulant.
- Emergency Red Flags: New-onset myoclonus, loss of consciousness, severe ataxia, or respiratory muscle weakness. Seek immediate medical attention.
Patient FAQ & Clinical Guidance
1. What does a positive MERRF mutation result mean?
A positive result identifies a known pathogenic MERRF gene variant associated with mitochondrial encephalomyopathy, meriting neurological correlation and family screening.
2. How is the blood sample collected and transported?
A certified DHA-licensed phlebotomist collects 4 mL of whole blood in an EDTA tube; the sample is shipped refrigerated (never frozen) with completed Form 20.
3. Can I stop my epilepsy medication before the test?
No, anti-epileptic drugs must never be discontinued without your physician's explicit approval, as abrupt cessation risks severe breakthrough seizures.
UAE Regulatory & Data Privacy Adherence
All patient data is processed in strict 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. Genomic information is encrypted, access-restricted, and never shared without explicit consent.
ISO 9001:2015 Certified | Cert: INT/EGQ/2509DA/3139
Clinical & Logistical Metadata
| Test Name | MERRF Mutation Detection Test (Myoclonic Epilepsy with Ragged Red Fibers) |
| Price (AED) | 2,500 |
| Turnaround Time | 10 working days |
| Sample Type / Matrix | Peripheral whole blood (4 mL EDTA tube) |
| Methodology Used | PCR Amplification + Sanger Validation |
| ICD-10-CM Code | G71.3 (Mitochondrial myopathy, not elsewhere classified) |
| LOINC Code | 83991-2 (MERRF mutation analysis) |
| DHA Facility License & Laboratory Address | License: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians