Test Price
1,400 AEDโ Home Collection Available
MERS (Middle East Respiratory Syndrome) (upE, ORF1a & ORF1b) Multiplex Detection and Differentiation (RNA Detection) Qualitative Test in UAE | 1,400 AED
Executive Summary & Core Metrics
Diagnostic Precision: 99.9% analytical sensitivity achieved through multiplex detection of upE, ORF1a, and ORF1b genes with reflex Whole Genome Sequencing (WGS) confirmation.
Accreditation: ISO 9001:2015 certified laboratory (Certificate: INT/EGQ/2509DA/3139) ensuring rigorous quality management standards.
Logistics: VIP mobile phlebotomy & temperature-controlled cold-chain home collection available daily from 8 AM to 11 PM.
Clinical Support: Complimentary post-result telephone consultation to interpret clinical implications.
Insurance: Direct insurance coverage verification via WhatsApp at +971 54 548 8731.
Test Overview & Methodology
This qualitative test utilizes a high-complexity multiplex Real-Time RT-PCR assay targeting the upE, ORF1a, and ORF1b genes of the Middle East Respiratory Syndrome Coronavirus (MERS-CoV). A reflexive Whole Genome Sequencing (WGS) protocol is activated upon positive detection to differentiate MERS-CoV from other circulating coronaviruses and identify potential genomic variants. This dual-methodology approach ensures the highest level of diagnostic fidelity for clinical management and epidemiological surveillance.
| Feature | Our Test (MERS Multiplex + WGS) | Closest Alternative (Single-target PCR) |
|---|---|---|
| Diagnostic Precision | 99.9% sensitivity; multiplex detection of 3 targets + confirmatory WGS | ~95% sensitivity; single gene target, risk of false negatives |
| Methodology | Multiplex Real-Time RT-PCR + Reflex Whole Genome Sequencing (WGS) | Conventional RT-PCR, no genomic differentiation capability |
| Turnaround Time | 36 hours (phone) / 48 hours (secure email) | 48-72 hours |
Physician Insight & Safety Protocols
โThe genomic differentiation of MERS-CoV from other respiratory viruses is vital for outbreak containment. Our multiplex approach targeting three distinct genetic regions aligns with international health regulations and ensures high diagnostic fidelity. A positive result requires immediate correlation with clinical symptoms and epidemiological links, while a negative result does not definitively exclude infection if sample quality was compromised. Consultation with an infectious disease specialist is strongly recommended for comprehensive interpretation.โ
โ Lina Osama Zaki Quteineh, Consultant Medical Genetics | DHA Registration ID: 9294403
Clinical Advisory & Medication Warning
โ ๏ธ Important Clinical Guidance
Do not discontinue prescribed medication without consulting your doctor. A MERS diagnosis requires comprehensive clinical correlation. Never alter antiviral or supportive therapies based solely on test results without direct physician guidance.
Exclusion Criteria & Emergency Red Flags
๐จ Contraindications for Home Collection
- Home collection is strictly contraindicated if the patient exhibits severe respiratory distress, cyanosis, or requires immediate hospital admission โ call emergency services immediately.
- Emergency red flags: sudden shortness of breath, bluish lips or face, chest pain, confusion, or inability to stay awake.
- All minors (<18 years) must be accompanied by a legal guardian; written parental consent is mandatory.
- Specimen integrity: avoid mouthwash, eating, or drinking for at least 2 hours before respiratory swab collection. Provide detailed clinical history to the attending phlebotomist.
Patient FAQ & Clinical Guidance
1. What is the MERS Multiplex RNA Detection test?
This qualitative multiplex PCR test detects MERS-CoV RNA by targeting upE, ORF1a, and ORF1b genes. It differentiates specific viral genetic markers from respiratory specimens such as sputum or nasopharyngeal swabs, providing a highly sensitive and specific diagnosis compared to single-target assays.
2. How should I prepare for sample collection?
You must sign a consent form, provide your recent clinical history, and avoid eating, drinking, or using mouthwash for 2 hours before respiratory swab collection. Our home collection team supplies viral transport medium to ensure specimen integrity.
3. When will I receive my results?
Results are delivered by phone within 36 hours and via secure email within 48 hours of sample collection. A comprehensive clinical interpretation guide accompanies your report to facilitate discussion with your physician.
UAE Regulatory & Data Privacy Adherence
Comprehensive Legal Compliance Framework
- Data Protection: All patient data is processed in strict compliance with Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL).
- Health Data Governance: Electronic health records and diagnostic data handling adhere to Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields.
- Medical Liability: Clinical testing safety and patient consent protocols strictly follow Federal Decree-Law No. 4 of 2016 on Medical Liability.
- DHA Licensing: This test is performed under the direct supervision of DHA Facility License Number 1143.
Clinical & Logistical Metadata
| Test Name | MERS (Middle East Respiratory Syndrome) (upE, ORF1a & ORF1b) Multiplex Detection and Differentiation (RNA Detection) Qualitative Test |
| Price (AED) | 1,400 |
| Turnaround Time | 36 hours (Phone) / 48 hours (Secure Email) |
| Sample Type / Matrix | Nasopharyngeal Swab / Sputum / Lower Respiratory Tract Aspirate |
| Methodology Used | Multiplex Real-Time RT-PCR (upE, ORF1a, ORF1b) + Reflex Whole Genome Sequencing (WGS) |
| ICD-10-CM Code | B97.21 |
| LOINC Code | 94531-1 |
| DHA Facility License & Laboratory Address | DNA Labs UAE | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DHA Facility License: 1143 |
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Available in Arabic, English, Hindi & Urdu
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HIPAA
All reports reviewed by DHA-Certified physicians