Test Price
2,800 AED✅ Home Collection Available
COL4A5 Gene Alport Syndrome, X-Linked Genetic Test in UAE | 2,800 AED | 2026 DHA Guidelines
تحليل جين COL4A5 لمتلازمة ألبورت المرتبط بالكروموسوم X في الإمارات | 2,800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).
- Premium Logistics: Hospital-Grade Home Collection with ISO Certified Cold-Chain Transport & VIP Mobile Phlebotomy.
- Clinical Guidance: Telephonic Post-Test Clinical Guidance for result interpretation by DHA-licensed specialists.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
الملخص التنفيذي
يوفر اختبار جين COL4A5 باستخدام تقنية التسلسل الجيني من الجيل التالي تشخيصًا دقيقًا لمتلازمة ألبورت المرتبطة بالكروموسوم X. يتمتع الاختبار بحساسية تشخيصية تصل إلى 99.9% من خلال مختبر معتمد وفقًا لمعايير ISO 9001:2015. نقدم خدمة سحب دم منزلي بمعايير سلسلة تبريد معتمدة، مع إمكانية التحقق من التأمين عبر واتساب. تتوفر استشارة طبية بعد الفحص لتفسير النتائج.
Test Overview
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. يكتشف فحص جين COL4A5 الطفرات المسببة لمتلازمة ألبورت المرتبطة بالكروموسوم X، مما يساعد في التشخيص المبكر لمشاكل السمع والكلى والعين.
| 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 #9834453 | May lack UAE regulatory recognition |
| Price (AED) | 2,800 – all inclusive | 3,500+ (often excludes counselling & logistics) |
| Sample Collection | Home / Clinic collection across UAE (Blood, Extracted DNA, or FTA card) | May require centre visit with limited home service |
Physician Insight & Safety Protocol
“As a DHA-licensed ENT 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 Warning: Do not discontinue any prescribed medication without consulting your doctor.
Safety & Exclusion Criteria
- Exclusion Criteria: Active untreated infection, inability to provide informed consent (for minors, valid legal guardian consent per UAE CDS Law 2026), 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.
Regulatory & Accreditation Standards
- Licensed by Dubai Health Authority (DHA) Facility #9834453
- ISO 9001:2015 Quality Management Certified (Cert: INT/EGQ/2509DA/3139)
- Compliant with Federal Decree-Law No. 41 of 2024, Article 87 – Genetic Privacy & Data Confidentiality
- Adheres to UAE PDPL (Personal Data Protection Law) and CDS Law 2026 provisions for minors
- All genetic data stored encrypted on UAE‑based servers; no cross‑border transfer without explicit consent
Frequently Asked Questions
Q: 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.
يحدد هذا الاختبار الطفرات المسببة للمرض في جين COL4A5، مما يؤكد متلازمة ألبورت المرتبطة بالكروموسوم X ويوجه الرعاية المتخصصة للكلى والسمع والعين.
Q: 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 paid hospital‑grade home collection 7 days a week from 8 AM to 11 PM with ISO‑certified cold‑chain logistics.
تستغرق النتائج من 3 إلى 4 أسابيع بعد استلام العينة، ونقدم خدمة سحب منزلي يوميًا من الثامنة صباحًا حتى الحادية عشرة مساءً مع سلسلة تبريد معتمدة.
Q: 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‑ consultation.
نقبل التأمين المباشر بعد التحقق عبر واتساب؛ ويشمل المبلغ 2,800 درهم الاستشارة الوراثية وسحب العينة وتحليل NGS والتقرير الشامل واستشارة ما بعد الفحص.
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التحقق من التغطية التأمينية
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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.
توقف عن التخمين. أرسل صورة من بطاقة التأمين ووصفة الطبيب إلى فريق التحقق المعتمد من هيئة الصحة بدبي عبر الواتساب. احصل على تحديث الحالة في دقائق.
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ISMS 27001:2022
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All reports reviewed by DHA-Certified physicians