Test Price
2,800 AED✅ Home Collection Available
FANCM Gene Fanconi Anemia Type M Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين FANCM لفحص فقر الدم فانكوني النوع M في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary (الملخص التنفيذي)
99.9% Diagnostic Sensitivity – Every sample is processed in our ISO 15189 & ISO 9001:2015 accredited laboratory, using Next Generation Sequencing (NGS) with full coverage of the FANCM gene, including copy number variations. UAE Ministry of Health & Prevention (MOHAP) compliance is strictly maintained.
Premium Home Collection (8 AM – 11 PM) – Complimentary VIP mobile phlebotomy with ISO-certified cold chain logistics. Your blood, DNA, or FTA card 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 Dr. Prabhakar Reddy (DHA License: 61713011) before release.
Insurance & Billing – Direct billing verification via WhatsApp at +971 54 548 8731. We coordinate with all major UAE insurers.
الضمان السريري: نقدم تحليل تسلسل الجيل التالي لجين FANCM وفق أعلى معايير الهيئة الاتحادية للرقابة النووية ووزارة الصحة، مع استشارة وراثية متكاملة قبل وبعد الفحص. جميع الإجراءات تلتزم بالمرسوم بقانون اتحادي رقم 41 لسنة 2024 (المادة 87) وقانون خصوصية البيانات الصحية.
Test Overview
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. In the UAE, this 2800 AED test is the most advanced screen for inherited susceptibility, delivering results in 3–4 weeks with clinical annotation tailored to local population variants.
يكشف هذا الفحص الشامل طفرات جين FANCM المسؤولة عن فقر الدم فانكوني النوع M، ويُعد المرجع الأول للعائلات الإماراتية لتأكيد التشخيص واتخاذ القرارات العلاجية.
| 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 & Clinical Correlation
“As a Consultant Hematologist with over two decades of experience in genetic anemia diagnosis, 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.”
— Dr. Prabhakar Reddy, DHA License 61713011 (Medical Director & Consultant Hematologist)
⚠ Medication Safety Notice
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; UAE Child Protection Safety (CDS) Law 2026 mandates parental/guardian consent with genetic counseling confirmation.
- 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 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. يوصى بهذا الفحص للعائلات التي لديها تاريخ من فشل النخاع العظمي أو تشوهات خلقية، لأنه يحدد الطفرات التي يمكن أن تنتقل عبر الأجيال.
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. يمكن جمع العينة إما عن طريق سحب دم وريدي بسيط من الذراع أو باستخدام بطاقة FTA عبر وخز الإصبع، وكلاهما غير مؤلم ويستغرق بضع دقائق فقط.
3. When will I get my results and what do they mean?
Results are released in 3–4 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 counselor explains every detail. تصدر النتائج خلال 3 إلى 4 أسابيع، والتقرير الإيجابي يتطلب إحالة فورية إلى أخصائي أمراض الدم، بينما النتيجة السلبية تستبعد الحالة بنسبة كبيرة مع شرح كامل من المستشار الوراثي.
دعم ثنائي اللغة متاح
التحقق من التغطية التأمينية
Check Insurance Coverage Instantly
Stop the guesswork. Send a photo of your Insurance Card and Doctor's Prescription to our DHA-Certified Verification Team on WhatsApp.
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