Test Price
110 AED✅ Home Collection Available
G-6-PD Quantitative Test in UAE | 110 AED | Clinical Enzyme Diagnostics by DNA Labs UAE
Executive Summary & Core Metrics
DNA Labs UAE delivers a precision G-6-PD Quantitative enzyme assay utilising kinetic UV spectrophotometry, the gold-standard methodology for measuring glucose-6-phosphate dehydrogenase activity in red blood cells. This test provides a definitive numerical result in U/g Hb, enabling accurate diagnosis of G6PD deficiency, severity stratification, and personalised trigger management. The service is backed by ISO 9001:2015 accredited processing (Cert: INT/EGQ/2509DA/3139) and operates under DHA Facility License 1143.
- Accuracy Guarantee: 99.9% diagnostic sensitivity via ISO-accredited kinetic UV assay.
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (daily 8 AM–11 PM).
- Clinical Guidance: Post-test telephonic interpretation by DHA-licensed physicians.
- Insurance: Direct billing verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The G-6-PD Quantitative Test measures the enzymatic activity of glucose-6-phosphate dehydrogenase in erythrocytes using kinetic UV spectrophotometry. This method continuously monitors NADPH production at 340 nm, delivering a precise quantitative result in units per gram of haemoglobin (U/g Hb). The assay is fully validated and approved by DHA and MOHAP for diagnostic use across the UAE.
| Feature | Our Test (Kinetic UV) | Closest Alternative (Qualitative Spot Test) |
|---|---|---|
| Precision & Output | Quantitative U/g Hb; exact enzyme activity level | Semi-quantitative fluorescent/non-fluorescent; no numeric value |
| Methodology | Kinetic UV spectrophotometry (gold standard, DHA/MOHAP approved) | Fluorescent spot test; prone to false positives during hemolysis |
| Turnaround Time | Same-day report (sample received by 4 pm Mon–Sat) | Variable, often exceeding 24 hours |
| Clinical Utility | Ideal for diagnosis, severity grading, and trigger management | Screening only; requires confirmatory testing |
Physician Insight & Safety Protocols
“A quantitative G-6-PD enzyme level provides essential objective data for diagnosing deficiency and assessing hemolytic risk. However, the result must always be correlated with the patient’s full clinical picture, including transfusion history, concurrent infections, and recent drug exposures. Precise enzyme values enable risk stratification and personalised avoidance of oxidative triggers, but no single laboratory parameter replaces a comprehensive medical evaluation.”
— Dr. Ajay Singh, General Practitioner, DHA Registration ID: 36234132
⚠️ Medication Safety Advisory
Never discontinue any prescribed medication without consulting your treating physician. G-6-PD deficiency requires careful drug review by a licensed clinician to avoid unintended hemolytic triggers.
Exclusion Criteria & Pre-Analytical Safeguards:
- Active hemolytic crisis or recent blood transfusion (within 3 months) may falsely lower activity – reschedule after full recovery.
- Sample must be collected in a lavender-top EDTA tube, immediately refrigerated (2–8°C), and never frozen.
- Haemolysed or clotted specimens will be rejected and require recollection.
- Patients with known G6PD deficiency should avoid oxidative drugs and foods (e.g., fava beans) before testing as directed by their physician.
🚨 Urgent Red Flags – Seek Immediate Medical Care:
- Sudden dark urine (cola-coloured) or new-onset jaundice
- Unexplained severe fatigue, back pain, or shortness of breath after exposure to oxidants, certain antibiotics, or infections
- Rapid heart rate, dizziness, or confusion
Patient FAQ & Clinical Guidance
1. What does a low G-6-PD enzyme level indicate?
A low G-6-PD enzyme level indicates a genetic deficiency that elevates the risk of red blood cell breakdown (hemolysis) upon exposure to oxidative triggers such as certain medications, infections, or fava beans. The quantitative result helps determine the severity of the deficiency and guides management planning.
2. How should I prepare for the G-6-PD quantitative test in UAE?
No special fasting is required. The test uses a simple refrigerated EDTA whole blood sample collected via our VIP mobile phlebotomy service. You may eat and drink normally before the collection. Ensure you inform your phlebotomist of any recent transfusions or acute illnesses.
3. Can I receive my G-6-PD results on the same day?
Yes, when your sample reaches our laboratory by 4 pm Monday through Saturday, you will receive a quantitative report the same day. Results are delivered securely via email or our patient portal, with telephonic follow-up from a DHA-licensed physician for interpretation.
UAE Regulatory & Data Privacy Adherence
🔒 Data Privacy & Clinical Safety Compliance
DNA Labs UAE operates under the regulatory oversight of the Dubai Health Authority (DHA Facility License 1143) and adheres to the highest standards of data protection and clinical safety as mandated by UAE federal law.
- Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL): All patient health information is collected, processed, and stored in full compliance with PDPL requirements, ensuring strict confidentiality and data security.
- Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields: Our digital health systems and telemedicine services operate within the secure framework defined by this law, safeguarding electronic medical records and communication channels.
- Federal Decree-Law No. 4 of 2016 on Medical Liability: Clinical testing, patient consent, and safety protocols are governed by this law, ensuring accountability and the highest standards of care throughout the diagnostic process.
Clinical & Logistical Metadata
| Test Name | G-6-PD Quantitative Test (Glucose-6-Phosphate Dehydrogenase Enzyme Activity) |
| Price (AED) | 110 AED |
| Turnaround Time | Same-day report (sample received by 4 PM Mon–Sat) |
| Sample Type / Matrix | EDTA whole blood (lavender-top tube), refrigerated 2–8°C, never frozen |
| Methodology Used | Kinetic UV Spectrophotometry (NADPH production at 340 nm) |
| ICD-10-CM Code | D55.0 |
| LOINC Code | 32531-0 |
| DHA Facility License & Laboratory Address | License No: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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