Test Price
2,800 AED✅ Home Collection Available
G6PD Deficiency Genetic Test in UAE | 2800 AED | DNA Labs UAE
Executive Summary & Core Metrics
Advanced next-generation sequencing (NGS) genetic test for comprehensive mutation analysis of the G6PD gene, directly elucidating hemolytic anemia due to G6PD deficiency. Delivers 99.9% diagnostic sensitivity, ISO 9001:2015 accredited processing, and mandatory pre-test genetic counselling. Includes VIP mobile phlebotomy with temperature-controlled cold-chain home collection (8 AM – 11 PM daily), direct insurance verification via WhatsApp (+971 54 548 8731), and post-test telephonic clinical guidance.
Test Overview & Methodology
The G6PD Deficiency Genetic Test uses next-generation sequencing to identify pathogenic variants in the full coding region of the G6PD gene, offering definitive molecular diagnosis for hemolytic anemia. This approach provides lifelong genetic information for personalized management and family screening, surpassing enzyme activity assays in diagnostic depth.
| Feature | Our NGS Test | Closest Alternative (Enzyme Activity) |
|---|---|---|
| Methodology | Next Generation Sequencing (NGS) – full gene analysis | Spectrophotometric enzyme activity assay |
| Diagnostic Precision | >99.9% mutation detection sensitivity | 80–95% in hemizygous males; can be normal during hemolysis |
| Sample & TAT | Blood, DNA, or FTA card – 3‑4 weeks | Whole blood – 1‑2 days |
| Clinical Utility | Definitive genotype, carrier & family risk, personalized avoidance guidance | Phenotype only; can be influenced by reticulocytosis/transfusion |
| Price | 2,800 AED | ~300–500 AED |
| ISO Accreditation | Yes (INT/EGQ/2509DA/3139) | Not always guaranteed |
Physician Insight & Safety Protocols
"A definitive molecular diagnosis of G6PD deficiency empowers patients and clinicians to make informed decisions about trigger avoidance and family counselling. While NGS offers unparalleled accuracy, it must be integrated with clinical history and hematological parameters for complete patient management."
— Lina Osama Zaki Quteineh, Consultant Medical Genetics (DHA: 9294403)
Medication Advisory
Do not alter or cease any prescribed medication regimen without explicit guidance from your treating physician. Some medications may trigger hemolysis in G6PD-deficient individuals; your doctor can advise on safe alternatives if needed.
Exclusion Criteria & Emergency Red Flags
- Patients currently in an acute hemolytic crisis (urgent medical attention required).
- Those who have received a blood transfusion within the last 3 months when providing whole blood or extracted DNA samples.
- Inability to give informed consent or participate in mandatory pre-test genetic counselling.
- Emergency Red Flags: Severe jaundice, dark urine, shortness of breath, or confusion — seek immediate medical help.
Patient FAQ & Clinical Guidance
1. What is the accuracy of this NGS test for G6PD deficiency?
The NGS-based G6PD gene analysis delivers 99.9% diagnostic sensitivity detecting all known pathogenic mutations precisely. This high-throughput sequencing comprehensively interrogates the entire G6PD coding sequence, rendering false‑negative results exceptionally rare. The assay is validated under ISO 9001:2015 conditions and is superior to enzyme activity tests that may be falsely normal in remitted hemolysis.
2. How long do results take, and what samples are accepted?
Results require 3 to 4 weeks, accepting blood, DNA, or FTA card sample types. Turnaround time begins upon receipt of a properly collected specimen and includes comprehensive bioinformatics analysis. For urgent clinical decisions, a preliminary report can be discussed; however, full interpretation integrates genetic counselling findings.
3. Is home collection available, and how does insurance coverage work?
Yes, we offer VIP mobile phlebotomy with temperature-controlled cold-chain home collection and direct insurance verification via WhatsApp for complete coverage facilitation. Our team operates from 8 AM to 11 PM across all Emirates with ISO‑certified logistics. Simply send your insurance card copy to +971 54 548 8731; we verify eligibility, handle pre‑authorization, and ensure minimal out‑of‑pocket expense.
UAE Regulatory & Data Privacy Adherence
- Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) – Governs all genetic information handled by our facility, ensuring strict confidentiality and patient consent protocols.
- Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields – Mandates secure digital handling of health records and telemedicine interactions.
- Federal Decree-Law No. 4 of 2016 on Medical Liability – Establishes clinical testing safety standards and patient consent requirements for all diagnostic procedures.
- ISO 9001:2015 Certified – Laboratory accreditation INT/EGQ/2509DA/3139, ensuring robust quality management systems across all workflows.
- DHA/MOHAP Standards – All procedures adhere to Dubai Health Authority and Ministry of Health and Prevention guidelines for genetic testing.
Clinical & Logistical Metadata
| Test Name | G6PD Deficiency Genetic Test (NGS) |
| Price (AED) | 2,800 |
| Turnaround Time | 3–4 weeks |
| Sample Type / Matrix | Whole Blood, Extracted DNA, or FTA Card (VIP Mobile Phlebotomy Available Daily 8 AM – 11 PM) |
| Methodology Used | Next-Generation Sequencing (NGS) – Full G6PD Gene Analysis |
| ICD-10-CM Code | D55.0 |
| LOINC Code | 32578-2 |
| DHA Facility License & Laboratory Address | DHA License 1143 — Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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ISMS 27001:2022
ISO Accredited
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All reports reviewed by DHA-Certified physicians