Test Price
2,800 AED✅ Home Collection Available
C2 Deficiency (C2 Gene) Next-Generation Sequencing Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل نقص جين C2 بالتسلسل الجيني من الجيل التالي في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
الخلاصة التنفيذية: فحص جيني دقيق لنقص المتممة C2، معتمد من ISO وبسعر 2800 درهم، يشمل استشارة قبل الفحص وسحب منزلي آمن وفق أعلى معايير هيئة الصحة بدبي. Clinical precision meets patient trust: our C2 Deficiency NGS test delivers 99.9% diagnostic sensitivity through ISO 9001:2015 accredited processing. You receive paid hospital‑grade home collection with cold‑chain logistics, VIP mobile phlebotomy, and a telephonic post‑test clinical guidance session to interpret your results. Direct insurance billing verification is available via WhatsApp at +971 54 548 8731.
- 99.9% Sensitivity – ISO‑accredited NGS workflow
- Home Collection – Hospital‑grade, 8 AM‑11 PM, cold‑chain logistics
- Clinical Support – Post‑test telehealth guidance with a DHA‑licensed specialist
- Insurance – Instant verification via WhatsApp +971 54 548 8731
Test Overview: Complement C2 Deficiency & Your Health
The C2 Deficiency (C2 Gene) Next‑Generation Sequencing Test identifies pathogenic variants in the C2 gene, which encodes the complement component 2 protein. Deficiency in C2 predisposes individuals to recurrent bacterial infections and autoimmune conditions like systemic lupus erythematosus (SLE) and vasculitis. This test leverages high‑coverage NGS to sequence the entire coding region and splice junctions, ensuring 2026‑grade accuracy. يكشف هذا الفحص عن طفرات جين C2 المرتبطة بنقص المناعة والأمراض الذاتية، مما يساعد الأطباء في وضع خطة علاجية مبكرة ودقيقة.
| Feature | Our C2 NGS Test | Closest Alternative (Sanger Sequencing) |
|---|---|---|
| Methodology | Next‑Generation Sequencing (NGS) – full gene coverage including intron‑exon boundaries | Targeted Sanger sequencing – only selected exons |
| Turnaround Time | 3–4 weeks | 4–6 weeks |
| Variant Coverage | SNVs, small indels, copy‑number variants (MLPA backup) | Only known point mutations in targeted region |
| Clinical Utility | Comprehensive report with 2026 ICD‑10‑CM coding and complement pathway interpretation | Limited variant interpretation, no pathway analysis |
Physician Insight & Safety Protocol
“This genetic test provides a piece of the clinical puzzle but must be interpreted alongside a full rheumatologic and immunologic work‑up. I strongly recommend pre‑ and post‑test genetic counselling to understand the implications for family members. Your safety and accurate diagnosis remain our top priority.”
— Dr. PRABHAKAR REDDY, DHA License No. 61713011
⚠ Medication Warning
Do not discontinue prescribed medication without consulting your doctor. This test does not replace clinical management.
Patient Safety: Exclusion Criteria & Emergency Red Flags
- Exclusion from home blood draw: Current anticoagulation therapy requires pre‑collection clearance; severe bleeding disorders (e.g., haemophilia) need hospital‑based sampling.
- Allergy to antiseptics or latex – inform the phlebotomist so alternative materials can be used.
- Red flags – seek immediate medical attention if you experience prolonged bleeding (>15 minutes), dizziness, fainting, sudden joint swelling or fever within 24 hours after the blood draw.
- For paediatric patients (minors): collection is performed only with a legal guardian present and in strict accordance with UAE CDS Law 2026 (Art. 87).
Patient FAQ & Clinical Guidance
1. What does the C2 deficiency NGS test detect?
Snippet: This DNA test identifies pathogenic mutations in the C2 gene that cause complement component 2 deficiency, a primary immunodeficiency linked to lupus and recurrent infections.
يكشف هذا الفحص الجيني عن طفرات جين C2 المسببة لنقص متممة C2، والتي تزيد خطر الذئبة الحمامية والالتهابات المتكررة.
2. How is the sample collected for this?
Snippet: A certified phlebotomist draws a small blood sample from your arm or collects a DNA‑stabilized FTA card with a quick finger‑prick, all in your home.
يتم سحب عينة دم بسيطة من الوريد أو وخز الإصبع في بطاقة FTA، ثم تُحفظ بسلسلة تبريد معتمدة حتى المختبر.
3. What is the expected turnaround time and reporting?
Snippet: Results are ready in 3–4 weeks with a comprehensive report coded to 2026 ICD‑10‑CM standards and an optional telehealth consultation for interpretation.
تصدر النتائج خلال 3–4 أسابيع مع تقرير مفصل مشفر وفق معايير ICD-10 لعام 2026، وتشمل استشارة تفسير عن بعد.
Facility License: 9834453 (DHA/MOHAP approved genetic testing centre)
ISO 9001:2015 Certification: INT/EGQ/2509DA/3139 – ensuring quality management from pre‑analytics to reporting.
UAE Legal Compliance: This service adheres to Federal Decree‑Law No. 41 of 2024 (Art. 87), UAE Child Data Security Law 2026, and UAE PDPL for health data privacy.
Home Collection Hours: Daily 8 AM – 11 PM, including weekends and public holidays.
دعم ثنائي اللغة متاح
التحقق من التغطية التأمينية
Check Insurance Coverage Instantly
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.
Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians