Test Price
4,800 AED✅ Home Collection Available
Bone Marrow Failure Syndrome Genetic Panel in UAE | 4800 AED | DHA Licensed
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Sequencing.
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection – Available daily from 8 AM to 11 PM.
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in Result Interpretation.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
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.
| 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 Protocols
“As a clinical geneticist, I emphasize that this panel delivers comprehensive molecular data. However, results must always be correlated with the patient’s full haematological history and physical exam. I strongly discourage any clinical decision-making without a dedicated genetic counselling session.”
— Lina Osama Zaki Quteineh, Consultant Medical Genetics (DHA ID: 9294403)Medication Advisory
Do not discontinue or modify any prescribed treatment, including immunosuppressants or growth factors, 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.
- Emergency Red Flags: Sudden onset of severe bruising, uncontrolled bleeding, high fever with neutropenia, or loss of consciousness – seek immediate emergency care.
Patient FAQ & Clinical Guidance
1. What does the Bone Marrow Failure Syndrome Genetic Panel test 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.
2. 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 specialized DNA stabilization tube, and you can resume normal activities immediately.
3. 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 geneticist) will review the integrated genetic report and schedule a dedicated appointment for interpretation and counselling.
UAE Regulatory & Data Privacy Adherence
- ✅ DHA-licensed facility operating under Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) – all patient data encrypted and anonymized.
- ✅ Compliant with Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields – secure electronic health records handling.
- ✅ Clinical safety and patient consent governed by Federal Decree-Law No. 4 of 2016 on Medical Liability.
- ✅ 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.
Clinical & Logistical Metadata
| Test Name | Bone Marrow Failure Syndrome Genetic Panel (NGS) |
| Price (AED) | 4,800 |
| Turnaround Time | 4–6 weeks |
| Sample Type / Matrix | Peripheral whole blood (2× EDTA tubes) |
| Methodology Used | Next-Generation Sequencing (Illumina platform) |
| ICD-10-CM Code | D61.9 (Aplastic anemia, unspecified) |
| LOINC Code | 81319-8 (Genetic panel for inherited bone marrow failure) |
| DHA Facility License & Address | License No. 1143 – Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE (DNA Labs UAE) |
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All reports reviewed by DHA-Certified physicians