Test Price
2,800 AED✅ Home Collection Available
COL4A5 Gene Alport Syndrome, X-Linked Genetic Test in UAE | 2,800 AED | DHA Licensed
Executive Summary & Core Metrics
Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection across all UAE emirates, daily from 8 AM to 11 PM.
- Clinical Guidance: Telephonic Post-Test Clinical Guidance for result interpretation by DHA-licensed specialists.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The COL4A5 NGS test identifies mutations in the COL4A5 gene responsible for X-linked Alport syndrome, guiding early intervention for hearing loss, renal disease, and ocular abnormalities. Next-Generation Sequencing provides full gene coverage with variant confirmation, surpassing traditional Sanger sequencing which may miss large deletions or cover only limited exons.
| Feature | Our Test (COL4A5 NGS) | Closest Alternative |
|---|---|---|
| Methodology | NGS (Next-Generation Sequencing) – full gene coverage with variant confirmation | Traditional Sanger Sequencing – limited exons, may miss large deletions |
| Turnaround Time | 3 to 4 Weeks | 6 to 8 Weeks |
| Accreditation | ISO 9001:2015, DHA Licensed Facility #1143 | May lack UAE regulatory recognition |
| Price (AED) | 2,800 – all inclusive | 3,500+ (often excludes counselling & logistics) |
| Sample Collection | VIP Mobile Phlebotomy home collection across UAE (peripheral whole blood, extracted DNA, or FTA card) | May require centre visit with limited home service |
Physician Insight & Safety Protocols
"As a DHA-licensed Consultant Medical Genetics specialist, I recognise the profound value of early genetic diagnosis in Alport syndrome. The COL4A5 NGS test empowers families with a definitive answer, yet it must always be correlated with audiological and renal assessments. I urge patients to involve a nephrologist and clinical geneticist for comprehensive care, and never to alter any medication regimen without direct medical supervision."
Important Medication Advisory
⚠️ Do not discontinue or alter any prescribed medication without direct consultation with your physician. This genetic test is for diagnostic guidance and does not replace ongoing medical treatment or specialist follow-up.
Safety & Exclusion Criteria
- Exclusion Criteria: Active untreated infection, inability to provide informed consent (for minors, valid legal guardian consent per Federal Decree-Law No. 4 of 2016 on Medical Liability), current anticoagulant therapy without physician clearance, known severe bleeding disorder.
- ER Red Flags (seek immediate medical care): Sudden severe hearing loss, macroscopic hematuria, acute flank pain, rapidly worsening hypertension, or sudden vision changes.
- For blood collection, inform the phlebotomist of all medications and supplements 48 hours prior.
- Pregnancy and lactation are not absolute contraindications, but clinical correlation is advised before testing.
Pre-Test Requirement: A detailed clinical history and a genetic counselling session to construct a pedigree chart of family members affected by COL4A5-related manifestations are mandatory.
Patient FAQ & Clinical Guidance
1. What does the COL4A5 gene test diagnose?
This test identifies disease-causing mutations in the COL4A5 gene, confirming X-linked Alport syndrome and directing targeted renal, auditory, and ophthalmological care.
2. How long do results take and is home collection available across the UAE?
The turnaround time is 3 to 4 weeks from sample receipt, and we offer VIP Mobile Phlebotomy home collection 7 days a week from 8 AM to 11 PM with ISO-certified cold-chain logistics across all emirates.
3. Is insurance accepted and what does the 2,800 AED fee include?
We support direct billing to most UAE insurers after verification via WhatsApp; the 2,800 AED covers genetic counselling, sample collection, NGS analysis, full clinical report, and a post-test consultation.
4. Who should consider this genetic test?
Individuals with a family history of Alport syndrome, unexplained haematuria, progressive hearing loss, or characteristic ocular abnormalities. Genetic counselling is recommended before testing.
5. What sample types are accepted and how should they be prepared?
Peripheral whole blood (EDTA tube), extracted DNA, or FTA card samples are accepted. No special preparation is required, but inform the phlebotomist of all medications 48 hours prior to collection.
UAE Regulatory & Data Privacy Adherence
Data Protection & Legal Compliance
- Licensed by Dubai Health Authority (DHA) Facility License Number: 1143
- ISO 9001:2015 Quality Management Certified (Cert: INT/EGQ/2509DA/3139)
- Compliant with Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL)
- Adheres to Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields
- All genetic data stored encrypted on UAE-based servers; no cross-border transfer without explicit consent
- Patient consent and safety protocols follow Federal Decree-Law No. 4 of 2016 on Medical Liability
Clinical & Logistical Metadata
| Test Name | COL4A5 Gene Alport Syndrome, X-Linked Genetic Test |
| Price (AED) | 2,800 |
| Turnaround Time | 3 to 4 Weeks |
| Sample Type / Matrix | Peripheral Whole Blood, Extracted DNA, or FTA Card |
| Methodology Used | Next-Generation Sequencing (NGS) with Variant Confirmation |
| ICD-10-CM Code | Q87.8 |
| LOINC Code | 94222-5 |
| DHA Facility License & Laboratory Address | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DHA License #1143 | DNA Labs UAE |
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All reports reviewed by DHA-Certified physicians