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Test Price

2,800 AED

✅ Home Collection Available

CD59 Gene Sequencing (NGS) Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines

تحليل تسلسل جين CD59 (NGS) في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي

الملخص التنفيذي: يوفر هذا التحليل المتقدم تسلسل جين CD59 بتقنية الجيل التالي (NGS) بدقة تشخيصية تبلغ 99.9% من خلال معامل معتمدة وفقًا لمعايير الآيزو، لتشخيص فقر الدم الانحلالي بوساطة CD59 مع أو بدون اعتلال الأعصاب المتعدد المناعي، مع خدمة سحب منزلي فاخرة واستشارة وراثية هاتفية بعد النتيجة.

Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Certified Processing (Cert: INT/EGQ/2509DA/3139).
Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection and VIP Mobile Phlebotomy (8 AM – 11 PM daily).
Clinical Guidance: Telephonic Post-Test Clinical Guidance with a DHA-licensed genetic counselor—interpretation of CD59 variant pathogenicity, family implications, and next steps.
Insurance Support: Direct Billing Verification via WhatsApp at +971 54 548 8731.

Overview – Why This Test Matters

CD59 gene sequencing identifies pathogenic variants causing a rare form of chronic hemolytic anemia with or without immune-mediated polyneuropathy—the only definitive way to confirm congenital CD59 deficiency. This NGS assay interrogates the entire coding region and splice sites, delivering actionable results for targeted therapies like anti‑C5 monoclonal antibodies and informed family planning. (يكتشف تسلسل جين CD59 الطفرات المسببة لفقر الدم الانحلالي المزمن النادر والاعتلال العصبي المناعي.)

Feature Our NGS Test Closest Alternative
Precision >99.9% analytical sensitivity for single nucleotide variants and small indels in CD59 Sanger sequencing may miss low-level mosaicism; limited to known exons only
Method Illumina-based NGS with orthogonal confirmation of all clinically significant variants PCR‑based fragment analysis or Sanger sequencing, slower turnaround
Speed 3–4 weeks definitive report, including variant classification per ACMG 2026 guidelines 6–8 weeks with potential reflex testing rounds

Physician Insight & Safety Protocol

“As a hematologist, I understand how unsettling chronic hemolysis and neuropathy can be. This genetic test provides the molecular clarity needed to differentiate CD59 deficiency from PNH or autoimmune conditions, so we can offer you precisely targeted therapy, not a guessing game. Please remember that results are just one piece of your clinical picture—always correlate with a specialist.”

— Dr. PRABHAKAR REDDY, DHA License No: 61713011

⚠ MEDICATION SAFETY NOTICE

Do not discontinue prescribed medication without consulting your doctor. Some drugs (e.g., erythropoietin, immunosuppressants) may interact with test interpretation or need gradual tapering. Self‑adjustment can trigger acute hemolytic crisis or neuropathic worsening.

Exclusion Criteria & Emergency Red Flags

  • Recent blood transfusion (<4 weeks) may mask hemolytic markers; defer test if possible.
  • Uncontrolled coagulopathy or severe thrombocytopenia — sample collection on FTA card preferred.
  • Active central nervous system infection (meningitis/encephalitis) — delay elective genetic workup.
  • ER red flags: Sudden severe hemolysis (dark urine, jaundice, dyspnea), ascending paralysis, or respiratory failure — go to emergency immediately, do not wait for test results.

Patient FAQ & Clinical Guidance

1. How accurate is this CD59 gene test, and can it detect all pathogenic variants?

Our NGS assay achieves >99.9% analytical sensitivity for single nucleotide variants and small insertions/deletions in the CD59 gene, with clinically validated bioinformatics pipeline. يبلغ معدل الحساسية التحليلية في فحصنا >99.9% لاكتشاف الطفرات النقطية والحذف الصغير في جين CD59 باستخدام تقنية الجيل التالي المعتمدة مخبريًا.

2. What sample types are accepted, and is home collection available in Dubai/Abu Dhabi?

We accept whole blood (lavender-top EDTA), extracted DNA, or a one‑drop blood FTA card, all collected by our VIP mobile phlebotomy team across UAE. تُقبل عينة الدم الكامل أو الحمض النووي المستخلص أو بطاقة FTA، مع خدمة سحب منزلي فاخرة تغطي دبي وأبوظبي وجميع الإمارات.

3. Will my insurance cover this, and how long until I get results?

Results are available in 3–4 weeks; our dedicated team verifies insurance pre‑approval via WhatsApp before scheduling, minimizing out‑of‑pocket surprises. تظهر النتائج خلال 3–4 أسابيع، ويتولى فريقنا التحقق من موافقة التأمين المسبقة عبر واتساب لضمان عدم وجود تكاليف مفاجئة.

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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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