Test Price
2,800 AED✅ Home Collection Available
CR1 Gene Deficiency Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين CR1 (نقص مستقبل المتممة الأول) في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Clinical Executive Summary
الفحص الجيني لجين CR1 لتشخيص نقص مستقبل المتممة الأول باستخدام تقنية التسلسل الجيني من الجيل التالي (NGS) بدقة مختبرية معتمدة من هيئة الصحة بدبي وشهادة الآيزو 9001.
- ✓ Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Certified Processing.
- ✓ Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection and VIP Mobile Phlebotomy.
- ✓ Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation by DHA-licensed consultants.
- ✓ Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview
The CR1 Gene Deficiency Genetic Test utilizes Next‑Generation Sequencing to screen for pathogenic variants in the complement receptor type 1 (CR1) gene, a key determinant in immune complex clearance and systemic lupus erythematosus (SLE) susceptibility. يُستخدم هذا التحليل لتأكيد نقص جين CR1 المرتبط باضطرابات المناعة الذاتية، ويُجرى على عينة دم أو DNA مستخلص.
| Feature | Our Test – CR1 Gene NGS | Closest Alternative – Complement Functional Panel (CH50/AH50) |
|---|---|---|
| Precision | 99.9% variant-level sensitivity; identifies exact mutation and carrier status | ~85% screening accuracy; cannot pinpoint genetic defect |
| Method | Next-Generation Sequencing (NGS) with bioinformatic filtering | Hemolytic assay (CH50 / AH50) |
| Speed | 3 – 4 Weeks | 1 – 2 Weeks |
Physician Insight & Safety Protocol
“As a clinical consultant, I emphasize that this genetic test provides critical information, but clinical correlation is mandatory. A negative NGS result does not exclude complement-mediated disease, and a positive variant must be interpreted alongside family history, complement protein levels, and autoimmune serology. Please use the post-test counselling we offer to integrate results safely into your care plan.”
— Dr. PRABHAKAR REDDY, DHA License No. 61713011
⚠️ Medication Safety Warning
Do not discontinue prescribed immunosuppressants, corticosteroids, or any medication without consulting your treating physician. Genetic test results are not a substitute for therapeutic decision-making.
Exclusion Criteria & Emergency Red Flags
- Sample Limitation: If you received a blood transfusion within 4 weeks, whole blood may not be suitable; an FTA card or extracted DNA sample is preferred.
- Paediatric Consent: Minors require guardian consent per UAE CDS Law 2026; genetic counselling session is mandatory before sample collection.
- ER Red Flags: Seek immediate emergency care if you experience sudden high fever, severe joint pain, new kidney dysfunction, or rapidly worsening lupus symptoms. This test does not replace urgent clinical evaluation.
Patient FAQ & Clinical Guidance
Q1: Is the CR1 gene NGS test the definitive way to diagnose complement receptor 1 deficiency?
Yes, the CR1 NGS test is the definitive molecular diagnostic for detecting pathogenic variants in the CR1 gene that cause complement receptor 1 deficiency. نعم، يعد تحليل جين CR1 بتقنية NGS الفحص الجزيئي القطعي لاكتشاف الطفرات المسببة لنقص مستقبل المتممة الأول.
Q2: How should I prepare for the sample collection, and what sample types are accepted?
You can provide a blood sample, extracted DNA, or a single drop of blood on an FTA card; a genetic counselling session is required beforehand to document family history. يمكنك تقديم عينة دم أو DNA مستخلص أو قطرة دم واحدة على بطاقة FTA؛ ويجب إجراء جلسة استشارة وراثية مسبقاً.
Q3: Will my health insurance cover the 2800 AED cost for this in the UAE?
Many UAE insurers cover medically necessary genetic testing; our team will verify your coverage via WhatsApp at +971 54 548 8731 before collection. تغطي العديد من شركات التأمين في الإمارات هذا الفحص؛ وسيتحقق فريقنا من تغطيتك عبر واتساب قبل سحب العينة.
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