Test Price
1,000 AED✅ Home Collection Available
Pan-Fungal Detection PCR Test in UAE | 1000 AED | DHA Licensed Laboratory
Executive Summary & Core Metrics
99.9% Diagnostic Sensitivity via ISO-Accredited Processing
Rapid molecular detection of a broad spectrum of fungal DNA directly from clinical specimens using real-time PCR technology. Results available within 2–4 days, enabling early targeted antifungal therapy. DHA-licensed facility with stringent quality control protocols. Hospital extraction required for CSF and tissue specimens. Telephonic post-test clinical guidance and direct insurance billing verification available.
Test Overview & Methodology
The Pan-Fungal Detection PCR Test is a molecular assay that identifies a broad range of fungal DNA from clinical specimens, enabling rapid diagnosis of invasive mycoses. The test targets conserved regions of fungal ribosomal DNA using real-time quantitative PCR (RT-qPCR), delivering high sensitivity and specificity compared to traditional culture methods that can take weeks.
| Feature | Pan-Fungal PCR (This Test) | Fungal Culture (Alternative) |
|---|---|---|
| Analytical Sensitivity | 99.9% with real‑time PCR targeting pan‑fungal rDNA | 50–70%; limited by slow growth and non‑viable organisms |
| Methodology | Automated nucleic acid extraction + RT‑qPCR (ISO 9001:2015 certified) | Conventional culture on selective agar; requires 2–4 weeks incubation |
| Turnaround Time | 2–4 days | Up to 4 weeks, delaying targeted therapy |
Physician Insight & Safety Protocols
A Note from Dr. Ajay Singh (DHA: 36234132)
"A positive pan‑fungal PCR result confirms the presence of fungal genetic material but must always be interpreted alongside clinical presentation, radiological findings, and full patient history. This test is a powerful diagnostic adjunct, not a standalone decision tool. I strongly recommend discussing your results with your treating physician to determine the most appropriate therapeutic pathway."
Medication Advisory
Do not discontinue any prescribed antifungal, immunosuppressant, or other medication without consulting your doctor. Abrupt changes can lead to disease progression, drug resistance, or severe adverse events. Always follow your physician's guidance regarding medication adjustments.
Exclusion Criteria & Emergency Red Flags
- Not intended for screening asymptomatic individuals without clinical suspicion of fungal infection.
- Patients with contraindications to blood draw (e.g., severe coagulopathy) require physician clearance prior to sampling.
- Seek emergency care if you develop high fever, severe shortness of breath, confusion, or rapidly spreading skin lesions after specimen collection.
- CSF and tissue collection must be performed by a licensed clinician under sterile hospital conditions.
Patient FAQ & Clinical Guidance
1. What is a Pan-Fungal PCR test and why is it ordered?
This molecular test rapidly detects DNA from over 50 fungal species in blood, bodily fluids, or tissue specimens. It is ordered when a healthcare provider suspects an invasive fungal infection, particularly in immunocompromised patients, to enable early diagnosis and targeted treatment within days rather than weeks.
2. How does the Pan-Fungal PCR compare to traditional fungal culture?
Our real‑time PCR assay delivers 99.9% analytical sensitivity and 100% specificity for the targeted pan‑fungal markers, significantly outperforming culture which can miss up to 50% of cases and requires 2–4 weeks for results. PCR provides actionable results in 2–4 days, enabling faster clinical decisions.
3. How should I prepare for sample collection?
No special preparation is required. For blood samples, a trained phlebotomist will collect the specimen under sterile conditions. For CSF or tissue specimens, collection must be performed in a hospital setting by a licensed clinician. All specimens are transported under strict cold-chain protocols directly to our ISO-accredited laboratory.
4. When will I receive my results and how are they delivered?
Results are typically available within 2–4 days from sample receipt. Reports are delivered electronically via secure channels, and telephonic post-test clinical guidance is available to discuss your results with a qualified healthcare professional.
UAE Regulatory & Data Privacy Adherence
Data Protection & Compliance Framework
This laboratory service operates 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. Clinical safety and patient consent procedures adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability. All test results are handled with strict confidentiality and secure data transmission protocols.
Clinical & Logistical Metadata
| Test Name | Pan-Fungal Detection PCR Test |
| Price (AED) | 1,000 |
| Turnaround Time | 2–4 days |
| Sample Type / Matrix | Whole blood (EDTA), CSF, sputum, sterile fluids, tissue in normal saline — Hospital Extraction Only – Sample collection is conducted strictly within an accredited hospital facility; mobile home phlebotomy is disabled for safety. |
| Methodology Used | Real-Time PCR (RT-qPCR) targeting fungal ribosomal DNA |
| ICD-10-CM Code | B49 (Unspecified mycosis) |
| LOINC Code | 60535-6 (Fungal organism identified in Specimen by Molecular method) |
| DHA Facility License & Laboratory Address | DHA License No: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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