Test Price
4,800 AED✅ Home Collection Available
Bone Marrow Failure Syndrome Genetic Panel in UAE | 4800 AED | 2026 DHA Guidelines
تحليل متلازمة فشل نخاع العظم في الإمارات | 4800 درهم | معتمد من هيئة الصحة بدبي
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Sequencing. دقة تشخيصية مضمونة 99.9% عبر تسلسل الجينوم المعتمد من الأيزو.
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain & VIP Mobile Phlebotomy. خدمة سحب الدم المنزلي المدفوعة عبر سلسلة تبريد معتمدة وفصد النخبة المتنقل.
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in Result Interpretation. إرشادات سريرية هاتفية بعد التحليل لتفسير النتائج.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731. التحقق المباشر من التغطية التأمينية عبر واتساب.
Clinical Overview
The Bone Marrow Failure Syndrome Genetic Panel uses next-generation sequencing (NGS) to detect pathogenic variants in genes linked to inherited bone marrow failure—such as FANCA, DKC1, TERT, and SBDS—guiding diagnosis, prognosis, and family planning. يستخدم هذا الفحص تسلسل الجيل التالي للكشف عن الطفرات المسببة لمتلازمات فشل نخاع العظم الوراثي لتوجيه التشخيص والتنبؤ وتنظيم الأسرة.
| Feature | Our Test (NGS Panel) | Closest Alternative (Single-Gene Sanger) |
|---|---|---|
| Precision | ≥99.9% analytical sensitivity; broad gene coverage | High per-gene accuracy but limited scope |
| Method | Next-Generation Sequencing (NGS) | Sanger Sequencing |
| Turnaround Time | 4–6 weeks | 3–4 weeks per gene (sequential) |
Physician Insight & Safety Protocol
“As a clinician, I understand that a bone marrow failure diagnosis can be overwhelming. This genetic panel provides data, but results must be interpreted within your full clinical picture. I strongly advise a detailed consultation with your haematologist before drawing conclusions.”
— Dr. PRABHAKAR REDDY, DHA License 61713011
⚠️ Medication Warning: Do not discontinue prescribed medication or alter your treatment plan without consulting your consultant haematologist or primary care physician.
Safety Exclusion Criteria & Emergency Red Flags
- Active systemic infection or acute febrile illness – reschedule collection.
- Pregnancy status (unless medically essential and ordered by specialist).
- Recent blood transfusion within 2 weeks may affect DNA yield – notify lab.
- ER Red Flags: Sudden onset of severe bruising, uncontrolled bleeding, high fever with neutropenia, or loss of consciousness – seek immediate emergency care.
UAE Regulatory Compliance & Accreditation
- ✅ DHA-licensed facility under Federal Decree-Law No. 41 of 2024, Art. 87 – patient data confidentiality.
- ✅ UAE Child Data Security Law 2026 – mandatory parental consent for minors.
- ✅ UAE PDPL compliant – all samples and reports anonymised & encrypted.
- ✅ ISO 9001:2015 Certified (Certificate: INT/EGQ/2509DA/3139) – Quality Management for Medical Laboratories.
- Pre-test requirement: A valid doctor’s prescription is required, except for pre-surgical clearance, pregnancy-related assessments, or travel abroad medical fitness certificates. Home collection order must be confirmed via WhatsApp.
Patient FAQ & Clinical Guidance
What does the Bone Marrow Failure Syndrome Genetic Panel for?
This NGS panel simultaneously analyses all major genes linked to inherited bone marrow failure syndromes, including Fanconi anaemia, dyskeratosis congenita, Diamond-Blackfan anaemia, and Shwachman-Diamond syndrome, providing a comprehensive molecular diagnosis. يحلل هذا الفحص الجيني جميع الجينات الرئيسية المرتبطة بمتلازمات فشل نخاع العظم الوراثي دفعة واحدة لتقديم تشخيص جزيئي شامل.
How should I prepare for the blood draw?
No fasting or special preparation is required; the phlebotomist will collect a peripheral blood sample in a special stabilised tube designed for DNA preservation, and you can resume normal activities immediately. لا يتطلب الفحص صيامًا أو تحضيرات خاصة، وسيتم سحب عينة دم محيطي في أنبوب حافظة للحمض النووي ويمكنك متابعة نشاطك فورًا.
How long before I receive my results, and who will explain them?
Results are typically available within 4–6 weeks; your referring physician (haematologist or general physician) will review the integrated genetic report and schedule a dedicated clinic appointment for interpretation. تظهر النتائج عادة خلال 4–6 أسابيع، ويقوم الطبيب المعالج (أخصائي أمراض الدم أو الطبيب العام) بمراجعة التقرير الجيني المتكامل وتحديد موعد لتفسيره.
دعم ثنائي اللغة متاح
التحقق من التغطية التأمينية
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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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All reports reviewed by DHA-Certified physicians