Test Price
2,800 AED✅ Home Collection Available
PEX13 Gene Zellweger Syndrome Genetic Test in UAE | 2800 AED | DHA Licensed
Executive Summary & Core Metrics
- 99.9% Diagnostic Sensitivity via ISO-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 Guidance in result interpretation.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
This NGS-based genetic test analyzes the entire PEX13 gene to detect mutations causing Zellweger spectrum disorders, enabling early diagnosis and family planning. The methodology employs next-generation sequencing with bioinformatic validation to achieve full gene coverage with variant-level resolution.
| Feature | Our Test (PEX13 NGS) | Closest Alternative (Sanger Sequencing) |
|---|---|---|
| Precision | Full gene coverage with variant-level resolution (99.9% sensitivity) | Targets single known mutations; may miss novel variants |
| Method | Next-Generation Sequencing (NGS) with bioinformatic validation | Capillary electrophoresis-based Sanger sequencing |
| Turnaround Time | 3 to 4 Weeks | 4 to 6 Weeks (limited by sequential analysis) |
Physician Insight & Safety Protocols
"As a consultant medical geneticist, I recognize the profound implications of a Zellweger spectrum diagnosis. This NGS test provides definitive molecular confirmation, yet results must always be interpreted alongside biochemical markers and clinical presentation. Genetic counselling is strongly recommended for families."
— Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
Medication Advisory
Never discontinue prescribed anticonvulsants or supportive therapy without consulting the treating physician. Abrupt cessation may precipitate severe neurological deterioration.
Exclusion Criteria & Emergency Red Flags
- Patients with active bleeding disorders or critical illness require medical clearance before blood collection.
- If the patient experiences seizures, severe hypotonia, or feeding difficulties, seek immediate emergency care at the nearest UAE hospital.
- This test is not a substitute for urgent biochemical or imaging studies in an acutely deteriorating infant.
Patient FAQ & Clinical Guidance
1. What is Zellweger syndrome and why is PEX13 gene testing necessary?
Zellweger syndrome, caused by PEX13 mutations, leads to severe neurological impairment; this test provides definitive genetic diagnosis and family planning.
2. How is the test performed and what sample is needed?
A small blood sample is collected via VIP Mobile Phlebotomy at your home between 8 AM and 11 PM. FTA cards are also accepted for archival purposes.
3. What is the turnaround time and how will I receive results?
Results are delivered within 3 to 4 weeks via secure email with telephonic guidance from our clinical team.
UAE Regulatory & Data Privacy Adherence
This test complies 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 follow Federal Decree-Law No. 4 of 2016 on Medical Liability. All genetic data is encrypted and processed under strict confidentiality protocols.
Clinical & Logistical Metadata
| Test Name | PEX13 Gene Zellweger Syndrome Genetic Test |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3 to 4 Weeks |
| Sample Type / Matrix | Peripheral whole blood (VIP Mobile Phlebotomy available) or FTA card |
| Methodology Used | Next-Generation Sequencing (NGS) with bioinformatic validation |
| ICD-10-CM Code | E88.9 (Disorder of peroxisomal function, unspecified) |
| LOINC Code | 91855-5 (Genetic testing mutation detection in PEX13) |
| 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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Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
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All reports reviewed by DHA-Certified physicians