Test Price
2,800 AED✅ Home Collection Available
PEX6 Gene Zellweger Syndrome Genetic Test in UAE | 2800 AED
Executive Summary & Core Metrics
- ✓ Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 15189‑accredited NGS processing.
- ✓ Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection, Available daily from 8 AM to 11 PM.
- ✓ Clinical Guidance: Telephonic Post-Test Clinical Interpretation with a DHA-licensed genetic counsellor.
- ✓ Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The PEX6 gene NGS test sequences the complete coding region and splice junctions to identify pathogenic variants responsible for Zellweger spectrum disorders, providing definitive molecular confirmation in 3 to 4 weeks. This test is performed under strict ISO 15189 accreditation, ensuring the highest diagnostic accuracy for peroxisomal biogenesis disorders.
| Feature | Our Test (ISO‑Certified NGS) | Closest Alternative |
|---|---|---|
| Methodology | Next‑Generation Sequencing of full PEX6 gene | Targeted mutation panel or single‑exon Sanger |
| Diagnostic Yield | >99% coverage of all coding variants | Limited to known hotspots (~60‑70%) |
| Turnaround Time | 3–4 Weeks | 4–8 Weeks |
| Pre‑test Support | Mandatory genetic counselling & pedigree chart | Often minimal or not included |
Physician Insight & Safety Protocols
“As a Consultant Medical Geneticist (DHA 9294403), I emphasize that a positive PEX6 result requires correlation with clinical and imaging findings; isolated genetic variants may not manifest the full syndrome. Pre‑ and post‑test genetic counselling is non‑negotiable. This test empowers families with answers, but it must be integrated into a comprehensive genetic evaluation.”
— Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
Safety Exclusion & Emergency Red Flags
- Exclusion Criteria: Patients unable to provide informed consent; individuals with active bleeding disorders unless accompanied by a physician; refusal of pre‑test genetic counselling.
- Emergency Red Flags: If you experience acute neurological deterioration (seizures, loss of consciousness, sudden inability to walk) or a severe reaction to the blood draw (swelling, difficulty breathing), go to the nearest Emergency Department immediately.
Medication Advisory
Do not discontinue prescribed medication without consulting your doctor. Some treatments may need adjustment based on genetic results; coordinate with your physician for safe management.
Patient FAQ & Clinical Guidance
1. What is the PEX6 gene test used for?
This DNA test identifies PEX6 gene mutations causing Zellweger spectrum disorders for accurate diagnosis and family planning. It analyzes the full PEX6 coding region using next‑generation sequencing, enabling detection of slight or novel variants often missed by narrower tests. Results help geneticists confirm a clinical suspicion and guide long‑term care and genetic counselling.
2. How is the sample collected?
Sample collection requires a standard blood draw or a finger‑prick onto an FTA card, performed by a DHA‑certified phlebotomist. You may choose our VIP Mobile Phlebotomy home collection service between 8 AM and 11 PM; a small amount of whole blood or DNA extracted from blood is sufficient. For young children, a heel‑prick onto a DNA storage card can be used with prior approval.
3. What is the turnaround time and price?
Results are delivered within 3 to 4 weeks for 2800 AED, with optional expedited processing available. The price includes pre‑test genetic counselling, sample collection kit, ISO‑standard laboratory analysis, and a post‑test telephone consultation to explain the report. Insurance pre‑approval can be verified instantly via WhatsApp.
UAE Regulatory & Data Privacy Adherence
Compliance Framework
All genetic data is processed and stored 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 adhere strictly to Federal Decree-Law No. 4 of 2016 on Medical Liability. Your genetic privacy is protected under the highest legal standards in the UAE.
Clinical & Logistical Metadata
| Test Name | PEX6 Gene Zellweger Syndrome Genetic Test (NGS) |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3–4 Weeks |
| Sample Type / Matrix | Peripheral Whole Blood or FTA Card (Dried Blood Spot) |
| Methodology Used | Next-Generation Sequencing (NGS) – Full Gene Sequencing |
| ICD-10-CM Code | E71.510 |
| LOINC Code | 69548-6 |
| 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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Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians