Test Price
2,800 AED✅ Home Collection Available
FANCM Gene Fanconi Anemia Type M Genetic Test | 2800 AED | DHA Licensed
Executive Summary & Core Metrics
99.9% Diagnostic Sensitivity — Every sample is processed in our ISO 15189 and ISO 9001:2015 accredited laboratory using Next Generation Sequencing (NGS) with full coverage of the FANCM gene including copy number variations. UAE MOHAP compliance is strictly maintained.
VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection — Complimentary home collection is available daily from 8 AM to 11 PM. Your peripheral blood sample is transported under continuous temperature monitoring ensuring pre-analytical integrity.
Post-Test Clinical Guidance — Telephonic interpretation session with a DHA-credentialed genetic specialist included. All results are reviewed and signed by Consultant Medical Genetics Lina Osama Zaki Quteineh (DHA Registration ID: 9294403) before release.
Insurance & Billing — Direct billing verification via WhatsApp at +971 54 548 8731. We coordinate with all major UAE insurers.
Test Overview & Methodology
The FANCM gene test is a comprehensive NGS-based analysis that detects germline mutations associated with Fanconi anemia type M, a chromosome breakage disorder causing bone marrow failure, congenital anomalies, and elevated cancer risk. This 2800 AED test delivers results in 3–4 weeks with clinical annotation tailored to local population variants.
| Feature | Our Test (DHA-Approved NGS) | Closest Alternative (Standard Panel) |
|---|---|---|
| Methodology | Full FANCM gene NGS + MLPA for deletions/duplications | Limited hotspot Sanger sequencing or multi-cancer panel without full FANCM coverage |
| Turnaround Time | 3–4 Weeks | 6–8 Weeks (often outsourced) |
| Diagnostic Yield | >99.9% analytical sensitivity, 98.5% clinical sensitivity for FANCM | ~85% sensitivity, misses copy number variants |
| Price | 2800 AED (all inclusive) | 3500–5000 AED (often plus consultation fees) |
| Interpretation | DHA Geneticist-backed report with Arab-family-specific ACMG classification | Generic bioinformatic pipeline, no regional variant annotation |
Physician Insight & Safety Protocols
“As a Consultant Medical Genetics specialist, I emphasize that a positive FANCM result must be interpreted in the context of clinical presentation, chromosome breakage studies, and family history. This NGS assay empowers families with precise carrier and predisposition information, but it is not a standalone diagnostic; comprehensive hematological follow-up remains the cornerstone of Fanconi anemia type M management.”
— Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
Medication Advisory
Do not discontinue any prescribed medication, including corticosteroids or androgen therapy, without explicit advice from your treating physician. Genetic results may take weeks; stopping supportive treatment abruptly can precipitate severe aplastic anemia.
Patient Safety Exclusion Criteria & Red Flags
- Exclusion: Patients who have received allogeneic hematopoietic stem cell transplantation within the last 6 months (donor DNA contamination).
- Exclusion: Active severe thrombocytopenia (<20×10⁹/L) — home phlebotomy may be delayed until medically optimized.
- Exclusion: Non-consenting minors; parental/guardian consent with genetic counseling confirmation is mandatory as per Federal Decree-Law No. 4 of 2016 on Medical Liability.
- Emergency Red Flag: If you experience uncontrollable bruising, bleeding, or signs of infection during the waiting period, seek immediate ER evaluation — do not wait for the genetic result.
Patient FAQ & Clinical Guidance
1. Why is the FANCM gene test recommended for my family?
This test identifies inherited mutations causing Fanconi anemia type M, a condition that leads to aplastic anemia and cancer susceptibility from childhood. Early detection enables life-saving surveillance and sibling donor matching.
2. How is the sample collected and does it hurt?
A certified nurse performs a simple venous blood draw from the arm, or you may provide a painless finger-prick blood spot on an FTA card. Both methods are completed in under 5 minutes under our VIP mobile phlebotomy service.
3. When will I get my results and what do they mean?
Results are released in 3 to 4 weeks. A positive report indicates a disease-causing variant that requires immediate hematology referral, while a negative result rules out the condition in most cases. Your genetic counselor explains every detail during a post-test telephonic session.
UAE Regulatory & Data Privacy Adherence
UAE Regulatory Compliance: This test and all associated data handling comply 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 adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability. Laboratory operations are licensed under DHA Facility License Number 1143.
Data Privacy: All genetic data is encrypted in transit and at rest. Access is restricted to authorized clinical personnel only. No data is shared with third parties without explicit patient consent as required by PDPL.
Clinical & Logistical Metadata
| Test Name | FANCM Gene Fanconi Anemia Type M Genetic Test |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3–4 Weeks |
| Sample Type / Matrix | Peripheral whole blood (venous or FTA card). VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection available daily from 8 AM to 11 PM. |
| Methodology Used | Next Generation Sequencing (NGS) with full gene coverage including MLPA for copy number variation detection |
| ICD-10-CM Code | D61.09 |
| LOINC Code | 21636-6 |
| DHA Facility License & Laboratory Address | DHA Facility License Number: 1143. Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE. Corporate Lab: DNA Labs UAE. |
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