Test Price
2,800 AED✅ Home Collection Available
CD59 Gene Hemolytic Anemia Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين CD59 لفقر الدم الانحلالي والاعتلال العصبي المناعي في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 certified processing and NGS technology.
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection and VIP Mobile Phlebotomy (8 AM – 11 PM).
- Clinical Guidance: Telephonic Post-Test Clinical Guidance for result interpretation and genetic counselling integration.
- Insurance: Direct Billing Verification via WhatsApp at +971 54 548 8731.
ملخص تنفيذي:
نضمن دقة تشخيصية تصل إلى 99.9٪ من خلال مختبر معتمد وفقًا لمعيار ISO 9001:2015. نقدم خدمة سحب الدم المنزلي المدفوعة مع سلسلة تبريد معتمدة، وإمكانية الاستشارة الهاتفية بعد الفحص. التحقق من التغطية التأمينية متاح عبر واتساب.
Comprehensive CD59 Gene Analysis via Next Generation Sequencing
This advanced genetic test screens for pathogenic variants in the CD59 gene, the molecular cause of CD59-mediated hemolytic anemia with or without immune-mediated polyneuropathy. In the UAE, this assay provides a definitive diagnosis, guides targeted management, and informs familial risk assessment under 2026 DHA standards.
| Feature | Our Test (NGS) | Closest Alternative (Sanger Sequencing) |
|---|---|---|
| Methodology | Next Generation Sequencing (NGS) – full gene coverage including deep intronic regions | Sanger sequencing – limited to exonic regions |
| Turnaround Time | 3 to 4 Weeks | 4 to 6 Weeks (variable) |
| Accreditation | ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139) | May lack international accreditation |
| Cost (AED) | 2800 | Variable, often higher without insurance |
| Comprehensive Reporting | Includes ACMG variant classification, clinical correlation, and genetic counselling session | Basic pathogenic/likely pathogenic reporting only |
Clinical Insight & Safety Protocol
From Dr. PRABHAKAR REDDY (DHA License: 61713011): "I understand the worry that comes with a possible genetic blood or nerve disorder. This NGS test offers clarity, but it must always be interpreted alongside your full clinical picture. Please do not hesitate to reach out to our genetic counsellor after receiving your results for a thorough explanation."
⚠️ Medication Warning: Do not discontinue prescribed medication without consulting your doctor. Sudden changes can provoke hemolytic crises or neurological deterioration.
Safety Exclusion Criteria & ER Red Flags
- This test is not indicated for healthy individuals without a personal or family history suggestive of CD59 deficiency.
- If you are currently experiencing acute hemolysis (dark urine, jaundice, severe fatigue) or rapidly progressive weakness/numbness, go to the nearest Emergency Department. Do not wait for genetic test results.
- ER Red Flags: sudden confusion, chest pain, difficulty breathing, loss of consciousness, or severe abdominal pain.
Frequently Asked Questions (Patient Guidance)
1. What does the CD59 genetic test detect and who should consider it?
This identifies pathogenic DNA variants in the CD59 gene that cause hemolytic anemia and immune-mediated nerve damage, helping confirm diagnosis in symptomatic patients and at-risk relatives.
يكشف هذا الاختبار عن الطفرات الممرضة في جين CD59 المسؤولة عن فقر الدم الانحلالي وإصابة الأعصاب المناعية، مما يساعد في تأكيد التشخيص للمرضى الذين تظهر عليهم الأعراض وللأقارب المعرضين للخطر.
2. How is the sample collected and is fasting required?
A small blood sample (or a few drops on an FTA card) is collected by our VIP mobile phlebotomist at your home or office between 8 AM and 11 PM, with no fasting needed and full cold-chain compliance.
تُسحب عينة دم بسيطة (أو بضع قطرات على بطاقة FTA) بواسطة أخصائي سحب الدم المتنقل في منزلك أو مكتبك بين الساعة 8 صباحًا و11 مساءً دون الحاجة للصيام، مع الامتثال الكامل لسلسلة التبريد.
3. How long does it take to receive the results and what support is included?
Results are delivered in 3 to 4 weeks, accompanied by a telephonic genetic counselling session to interpret your report and plan next steps with your referring physician.
تُصدر النتائج خلال 3 إلى 4 أسابيع، مصحوبة بجلسة استشارة وراثية هاتفية لتفسير التقرير وتخطيط الخطوات التالية مع طبيبك المعالج.
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
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HIPAA
All reports reviewed by DHA-Certified physicians