Test Price
750 AED✅ Home Collection Available
Pan Fungal (RNA Detection) Qualitative Test in UAE | 750 AED | DHA Licensed
Executive Summary & Core Metrics
Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 accredited molecular processing (Cert: INT/EGQ/2509DA/3139). Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection for blood samples (available daily 8 AM‑11 PM); tissue biopsy requires hospital extraction only. Clinical Guidance: Complimentary telephonic post‑test result interpretation by senior clinical team. Insurance: Direct billing verification via WhatsApp at +971 54 548 8731.
Test Overview & Methodology
The Pan Fungal (RNA Detection) Qualitative Test rapidly identifies a broad spectrum of fungal pathogens directly from tissue, blood or respiratory specimens using real‑time RT‑PCR and whole genome sequencing (WGS). This molecular method detects RNA from a wide range of fungal genera — including Aspergillus, Candida, Mucorales and rare moulds — in a single assay, making it indispensable for immunocompromised patients where swift treatment decisions are critical.
| Feature | Our Test (DNA Labs UAE) | Conventional Fungal Culture |
|---|---|---|
| Molecular Precision | Real‑Time RT‑PCR + WGS | Growth‑based, dependent on viable organisms |
| Diagnostic Sensitivity | 99.9% | 50–75% (varies by species) |
| Turnaround Time | 36–48 hours | 7–21 days |
Physician Insight & Safety Protocols
“This pan‑fungal RNA assay harnesses molecular genetics to rapidly detect a broad range of fungal pathogens, enabling precise diagnosis even in the immunocompromised. However, a negative result does not entirely rule out infection, especially if prior antifungal therapy has been administered. Integrating this test with clinical and histopathological findings is essential. Our team is dedicated to supporting your journey with clear, empathetic guidance.”
— Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
⛔ Medication Safety Advisory
Do not discontinue any prescribed antifungal or immunosuppressive medication without prior consultation with your treating physician. Abrupt cessation may precipitate disease reactivation or acute deterioration. All clinical procedures comply with Federal Decree-Law No. 4 of 2016 on Medical Liability.
Exclusion Criteria & ER Red Flags
- Exclusion: Severe uncorrected coagulopathy (INR >2.0, platelets < 50×10⁹/L) that precludes safe biopsy; inability to provide informed consent.
- ER Red Flags: New‑onset confusion, meningismus, acute visual loss, or haemodynamic instability in a patient with suspected fungal infection — proceed immediately to the nearest emergency department.
- Exclusion: Active bleeding at the proposed biopsy site or concurrent use of high‑dose anticoagulants that cannot be temporarily withheld under medical supervision.
Patient FAQ & Clinical Guidance
1. What does the Pan Fungal RNA Test detect that a standard culture cannot?
The Pan Fungal RNA directly amplifies fungal ribosomal RNA from tissue or blood, providing a 99.9% sensitivity result within 36–48 hours, even when fungi are non‑viable or fastidious, unlike culture that relies on growth and can take 1‑3 weeks. This molecular method detects RNA from a wide range of fungal genera — including Aspergillus, Candida, Mucorales and rare moulds — in a single assay, making it indispensable for immunocompromised patients where swift treatment decisions are critical.
2. Is fasting or any special preparation required before sample collection?
No fasting or dietary restrictions are needed; however, you must provide a signed consent form and a detailed clinical history including all current antifungal, antibiotic and immunosuppressive medications. For tissue biopsies, the site will be prepared under sterile conditions by the attending physician or our mobile phlebotomy team. If a blood sample is used, standard venepuncture is performed. Continue all prescribed drugs unless your doctor advises otherwise.
3. How quickly will I receive my results and who interprets them?
Your physician will receive a comprehensive PDF report within 4 working days (48 hours) by email, while a preliminary verbal result can be shared by phone within 36 hours, followed by a complimentary tele‑consultation with our clinical team for interpretation. The report includes the detected fungal RNA targets, semi‑quantitative data, and correlation with susceptibility markers when applicable. All data is handled in strict compliance with UAE Personal Data Protection Law (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields.
UAE Regulatory & Data Privacy Adherence
Data Protection & Compliance
All personal and health data processed through this test is governed by 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. Clinical safety and patient consent protocols adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability. Laboratory operations are conducted under DHA Facility License No. 1143 at Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE. For any privacy concerns, contact our Data Protection Officer at +971 54 548 8731.
Clinical & Logistical Metadata
| Test Name | Pan Fungal (RNA Detection) Qualitative Test |
| Price (AED) | 750 AED |
| Turnaround Time | 36–48 Hours |
| Sample Type / Matrix | Blood, Tissue, or Respiratory Specimen (tissue biopsy requires hospital extraction) |
| Methodology Used | Real‑Time RT‑PCR & Whole Genome Sequencing |
| ICD-10-CM Code | B49 (Fungal infection, unspecified) |
| LOINC Code | 60571-3 (Fungal organism identified in Specimen by PCR) |
| DHA Facility License & Laboratory Address | DHA License No. 1143 | DNA Labs UAE | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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