Test Price
2,800 AED✅ Home Collection Available
Fanconi Anemia Type D2 (FANCD2) Gene Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل فحص جين FANCD2 المرتبط بفقر الدم فانكوني النوع الثاني في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
يقدم تحليلنا لجين FANCD2 بتقنية التسلسل الجيني (NGS) تشخيصاً دقيقاً لفقر الدم فانكوني النوع الثاني وفق أعلى معايير هيئة الصحة بدبي والجهات التنظيمية.
- 99.9% Diagnostic Sensitivity – ISO-accredited processing with next-generation sequencing for every coding region and splice site.
- Premium Home Collection – ISO-certified cold-chain logistics, VIP mobile phlebotomy (8 AM – 11 PM) at no extra clinical cost.
- Telephonic Post-Test Guidance – DHA-licensed physicians explain results and clinical next steps.
- Insurance Direct Billing – WhatsApp verification at +971 54 548 8731.
Clinical Overview
This next-generation sequencing (NGS) test analyzes the entire FANCD2 gene for pathogenic variants causing Fanconi anemia type D2, a DNA repair disorder with progressive bone marrow failure and elevated cancer risk. يكشف الفحص عن الطفرات الجينية في جين FANCD2 المرتبط بفقر الدم فانكوني.
| Feature | Our FANCD2 NGS Test | Closest Alternative (Sanger Sequencing) |
|---|---|---|
| Precision | >99.9% diagnostic sensitivity for all coding variants | Limited to targeted hotspot regions |
| Methodology | Full gene NGS with copy-number variant detection | Sequential exon sequencing; low CNV resolution |
| Turnaround Time | 3–4 weeks | 6–8 weeks |
Physician Insight & Patient Safety
“As a DHA-licensed physician, I remind you that this advanced genetic test provides vital information, but its interpretation must always be correlated with your personal and family clinical history. A negative result does not entirely rule out other forms of bone marrow failure, so continue regular follow-ups. Please reach our genetic counselling team to fully understand your results before making any medical decisions.”
Dr. PRABHAKAR REDDY, DHA License: 61713011
Important Medication Warning
Do not discontinue prescribed medication, supplements, or supportive care without consulting your doctor. This test is for diagnostic insight only and should never replace ongoing clinical management.
Exclusion Criteria & Emergency Red Flags
- Active severe infection or febrile illness – postpone non‑urgent genetic testing until stabilised.
- Recent blood transfusion (within 4 weeks) may interfere with DNA extraction from whole blood; use DNA FTA card or extracted DNA in such cases.
- If you experience sudden bleeding, high fever >38.5°C, or extreme fatigue, seek immediate emergency care – do not wait for test results.
- This test is not a substitute for urgent haematological evaluation in acutely ill patients.
Patient FAQ & Clinical Guidance
1. ما هي دواعي إجراء فحص جين FANCD2؟ (Why is this test performed?)
This FANCD2 gene test confirms or rules out Fanconi anemia type D2 in patients with bone marrow failure, congenital anomalies, or a family history of the condition, and also supports carrier screening and reproductive planning.
يُستخدم الفحص لتأكيد تشخيص فقر الدم فانكوني النوع الثاني عند المرضى الذين يعانون من فشل نخاع العظم أو التشوهات الخلقية، ولتقدير خطر انتقال المرض وراثياً.
2. كيف يتم جمع العينة وما فترة الانتظار؟ (How is the sample collected and what is the turnaround time?)
Our home phlebotomy team collects a single blood sample, extracted DNA, or a dried blood spot on an FTA card, with the full NGS result delivered in 3 to 4 weeks along with a clinical interpretation report.
تُسحب العينة بواسطة فريقنا المتنقل باستخدام الدم الكامل أو بطاقة FTA، وتصدر النتيجة خلال 3 إلى 4 أسابيع مع تقرير تفسيري سريري.
3. هل يمكن للفحص اكتشاف حالات وراثية أخرى؟ (Does this test detect other genetic conditions?)
The assay is specifically designed for the FANCD2 gene and Fanconi anemia type D2; it does not screen for other bone marrow failure syndromes unless explicitly expanded to a broader panel, which must be discussed with your genetic counsellor.
الفحص مخصص حصراً لجين FANCD2 ولا يكشف عن اضطرابات جينية أخرى ما لم يُطلب فحص شامل، ويجب مناقشة الخيارات الموسعة مع المستشار الوراثي.
Pre‑ Requirements
A genetic counselling session is mandatory to draw a detailed pedigree chart of family members affected by Fanconi anemia type D2. Please share all relevant clinical records before sample collection.
Acceptable sample types: Whole blood (EDTA), extracted DNA, or one drop of blood on an FTA card. No fasting or medication adjustments are required; maintain your usual health regimen unless advised by your physician.
Compliant with Federal Decree-Law No. 41 of 2024 (Art. 87), CDS Law 2026 (Minors), and UAE PDPL. Genetic data handled with ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139) certified privacy. Facility License: 9834453. DHA‑approved methodology: NGS, full gene coverage.
ICD‑10‑CM 2026: D61.01, Z14.8, Z13.7 | LOINC: 101516-4
24/7 WhatsApp Support: +971 54 548 8731
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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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