Test Price
1,200 AED✅ Home Collection Available
CEBPA Full Gene Mutation Analysis in UAE – 1200 AED – DHA Licensed Laboratory
Executive Summary & Core Metrics
Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).
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 by DHA-licensed specialists.
Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Price: 1,200 AED | Turnaround Time: 5–6 working days from sample receipt.
Test Overview & Methodology
The CEBPA Full Gene Mutation Analysis is a targeted genetic test that sequences the entire coding region of the CEBPA gene to detect somatic mutations with high sensitivity. In the UAE, this assay is primarily utilised for risk stratification and prognosis in acute myeloid leukaemia (AML) and other myeloid disorders, delivered under DHA‑standardised protocols.
This single‑gene Sanger sequencing approach provides definitive confirmation of biallelic or monoallelic mutations, which are critical for classifying AML subtypes and guiding treatment intensity. Results are correlated with cytogenetics and clinical presentation to inform therapeutic decisions.
| Feature | Our Test (DNA Labs UAE) | Closest Alternative |
|---|---|---|
| Methodology | Sanger Sequencing (gold standard for single‑gene confirmation) | NGS Myeloid Panel (multi‑gene, may miss rare variants) |
| Turnaround Time | 5 – 6 days | 10 – 14 days |
| Price | 1,200 AED | 2,500 – 4,000 AED |
| Accreditation | DHA‑licensed facility (License: 1143), ISO 9001:2015 | Variable; may lack UAE‑specific clinical validation |
| Sample / Pre‑analytics | Peripheral Blood (EDTA); Doctor’s prescription mandatory | Often requires bone marrow aspirate for comprehensive panels |
Physician Insight & Safety Protocols
Lina Osama Zaki Quteineh | Consultant Medical Genetics | DHA Registration ID: 9294403: “I understand that confronting a possible blood disorder can be distressing. The CEBPA mutation analysis is a powerful clinical tool that provides clear prognostic information, helping us personalise treatment strategies for conditions like AML. I urge patients to review results with their specialist, as this genetic finding is only one piece of the complete clinical puzzle.”
Important Medication Warning
Do not discontinue prescribed medication without consulting your doctor. Genetic test results are not a substitute for ongoing haematological care and do not authorise therapy changes on their own.
Exclusion Criteria & ER Red Flags
- Exclusion: Not recommended for individuals who have received a blood transfusion within the last 2 weeks (may confound germline mutation detection).
- Exclusion: Active chemotherapy or recent haematopoietic stem cell transplant may affect somatic mutation assessment; consult your physician about optimal timing.
- Prescription Note: A valid doctor's prescription is mandatory. Prescription waiver is strictly not applicable for pre‑surgical clearance, pregnancy‑related screening, or travel fitness certificates.
- Red Flags – Seek Immediate Medical Attention: If you develop worsening fatigue, unexplained bruising or bleeding, persistent fever, or recurrent infections, please visit the nearest emergency department.
Patient FAQ & Clinical Guidance
1. What is the CEBPA Full Gene Mutation Analysis used for?
Snippet: CEBPA mutation testing classifies acute myeloid leukaemia (AML) subtypes and predicts favourable treatment response, directly influencing therapeutic intensity and stem cell transplant decisions.
The test sequences the entire CEBPA gene, identifying both single‑base and small insertion/deletion mutations, which are critical prognostic markers in AML and, rarely, in other myeloid neoplasms. Results must always be correlated with cytogenetics and clinical findings.
2. How should I prepare for the blood sample collection?
Snippet: No fasting or special preparation is required; simply bring the original doctor’s prescription and a valid Emirates ID to your appointment.
Our phlebotomist will collect 3 mL of peripheral blood in an EDTA tube. If you have undergone a recent transfusion, inform the booking team so we can schedule the draw accordingly. Home collection is available from 8 AM to 11 PM via WhatsApp booking.
3. Will my genetic data be kept confidential under UAE law?
Snippet: Absolutely; your sample and genomic data are fully protected under Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields.
All personal health information is governed by strict access controls. Our laboratory complies with ISO 9001:2015 standards and mandates informed consent for genetic testing. For more data privacy inquiries, contact our DHA‑licensed data protection officer via WhatsApp.
UAE Regulatory & Data Privacy Adherence
All testing performed at DNA Labs UAE complies with Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. Clinical safety and patient consent follow Federal Decree-Law No. 4 of 2016 on Medical Liability. Our facility is DHA-licensed (License No. 1143) and ISO 9001:2015 certified (Cert: INT/EGQ/2509DA/3139). Genetic data is stored, processed, and transmitted through encrypted channels with role-based access controls.
Clinical & Logistical Metadata
| Test Name | CEBPA Full Gene Mutation Analysis |
| Price (AED) | 1,200 AED |
| Turnaround Time | 5 – 6 working days from sample receipt |
| Sample Type / Matrix | Peripheral Blood – 3 mL in EDTA tube (lavender top) |
| Methodology Used | Sanger Sequencing (full coding region) |
| ICD-10-CM Code | C92.00, D46.9, Z15.09 |
| LOINC Code | 101543-4 |
| DHA Facility License & Laboratory Address | DHA License: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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