Test Price
2,800 AEDโ Home Collection Available
PEX10 Gene Zellweger Syndrome Spectrum Genetic Test in UAE
Executive Summary & Core Metrics
Diagnostic precision for Peroxisome Biogenesis Disorder-Zellweger Spectrum. Accuracy Guarantee of 99.9% Diagnostic Sensitivity via ISO 9001:2015 Certified Processing. Premium Logistics include VIP Mobile Phlebotomy and Temperature-Controlled Cold-Chain Home Collection (Available daily from 8 AM to 11 PM). Telephonic Post-Test Clinical Guidance provided. Direct Billing Verification available via WhatsApp +971 54 548 8731. This test adheres to Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL), Federal Law No. 2 of 2019 on Health ICT, and Federal Decree-Law No. 4 of 2016 on Medical Liability.
Test Overview & Methodology
The PEX10 Gene Zellweger Syndrome Spectrum NGS Test utilizes Next-Generation Sequencing to identify pathogenic variants in the PEX10 gene, responsible for peroxisome biogenesis. This test confirms a clinical diagnosis of Zellweger Spectrum Disorder, a severe neurological condition, enabling personalized management and familial genetic counseling. Pre-test genetic counseling to create a pedigree chart is recommended.
| Feature | Our Test (PEX10 NGS) | Alternative (Standard) |
|---|---|---|
| Precision & Depth | 99.9% Diagnostic Sensitivity, 100x Read Depth | ~85% Sensitivity, 20x Read Depth |
| Methodology | NGS with AI-Enhanced Bioinformatics & LC-MS/MS Confirmation | Sanger Sequencing |
| Turnaround Time | 3 to 4 Weeks | 8 to 12 Weeks |
Physician Insight & Safety Protocols
"As a Consultant Medical Genetics, I emphasize that a PEX10 genetic result must be correlated with the clinical phenotype, very-long-chain fatty acid profiles, and neuroimaging for a definitive diagnosis and prognosis. Genetic counseling is essential for families considering this test." โ Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403.
Critical Medication Notice
Do not discontinue prescribed medication without consulting your doctor. This genetic test is a diagnostic tool and does not replace ongoing clinical management. Always follow your physician's guidance regarding medication adjustments.
Patient Safety & Exclusion Criteria
- Exclusion Criteria: No test will be performed on minors without strict adherence to UAE federal laws and valid legal guardian consent. Patients on anticoagulant therapy should consult their physician before blood collection.
- Emergency Red Flags: If the patient exhibits acute neurological decompensation (status epilepticus, unresponsiveness, central apnea), seek immediate emergency care; do not wait for genetic test results.
Patient FAQ & Clinical Guidance
1. What is the clinical purpose of the PEX10 Zellweger syndrome test?
This advanced NGS-based genetic test identifies disease-causing mutations in the PEX10 gene to confirm a clinical diagnosis of Zellweger Spectrum Disorder, enabling personalized management and familial genetic counseling. Pre-test genetic counseling to create a pedigree chart of affected family members is recommended prior to sample collection.
2. How do I prepare for the test and what sample types are required?
The test accepts Blood (Whole Blood, EDTA), Extracted DNA, or FTA Card samples. Our VIP home collection team ensures proper handling with temperature-controlled cold-chain logistics. Patients must complete the pre-test genetic counseling session and share any medication or supplement lists from their primary physician before specimen collection.
3. How long does it take to receive the test results?
The turnaround time for the PEX10 gene sequencing test is 3 to 4 weeks. Results are delivered electronically and include a detailed clinical interpretation report. Post-test telephonic guidance is available from our clinical genetics team.
4. How can I verify my insurance coverage for this test?
To verify insurance coverage for the PEX10 Zellweger syndrome test, please send your insurance card via WhatsApp to +971 54 548 8731 for direct and immediate verification.
UAE Regulatory & Data Privacy Adherence
Regulatory Compliance & Data Protection
DNA Labs UAE operates under DHA Facility License Number 1143. We strictly adhere to 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. Our laboratory processes comply with Federal Decree-Law No. 4 of 2016 on Medical Liability, ensuring patient consent, clinical safety, and data confidentiality at all stages.
Clinical & Logistical Metadata
| Test Name | PEX10 Gene Zellweger Syndrome Spectrum Genetic Test (NGS) |
| Price (AED) | 2,800 |
| Turnaround Time | 3 to 4 Weeks |
| Sample Type / Matrix | Blood (Whole Blood, EDTA), Extracted DNA, or FTA Card |
| Methodology Used | Next-Generation Sequencing (NGS) with AI-Enhanced Bioinformatics and LC-MS/MS Confirmation |
| ICD-10-CM Code | E71.510 |
| LOINC Code | 81313-5 |
| DHA Facility License & Laboratory Address | DHA License: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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Stop the guesswork. Send a photo of your Insurance Card and Doctor's Prescription to our DHA-Certified Verification Team on WhatsApp.
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All reports reviewed by DHA-Certified physicians