Test Price
2,800 AED✅ Home Collection Available
FANCE Gene (Fanconi Anemia Type E) Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين FANCE لأنيميا فانكوني من النوع E بتقنية التسلسل الجيني (NGS) في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary / ملخص تنفيذي
- ✓ Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).
- ✓ Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection and VIP Mobile Phlebotomy (8 AM – 11 PM).
- ✓ Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation by DHA-licensed clinicians.
- ✓ Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
تحليل جيني دقيق ومعتمد بتقنية NGS بمعدل حساسية 99.9% للتغيرات المرضية في جين FANCE، مع خدمة السحب المنزلي المعقمة ونقل العينة بسلسلة تبريد موثوقة ومراجعة سريرية من أطباء مرخصين من هيئة الصحة بدبي إضافة إلى دعم التأمين المباشر عبر واتساب.
Overview
This test screens the FANCE gene for pathogenic variants causing Fanconi Anemia type E – a hereditary bone marrow failure syndrome with cancer predisposition. It combines next-generation sequencing (NGS) and advanced bioinformatic analysis to deliver clinically actionable results for early diagnosis, family screening, and personalized management.
يُستخدم هذا التحليل للكشف عن التغيرات الجينية في جين FANCE المسببة لأنيميا فانكوني من النوع E، وهو اضطراب وراثي نادر يؤثر على نخاع العظم ويزيد خطر الإصابة بالسرطان، مما يوفر معلومات حاسمة للتشخيص المبكر والتخطيط الأسري.
| Feature | Our Test (DNA Labs UAE) | Closest Alternative (Sanger Sequencing) |
|---|---|---|
| Technology | NGS – full gene sequencing with CNV detection | Sanger sequencing – targeted exon-by-exon |
| Turnaround Time | 3 to 4 Weeks | 5 to 7 Weeks |
| Detection Rate | >99% of pathogenic variants (single nucleotide & copy number) | ~95% (misses large deletions/duplications) |
| Home Collection | Included (ISO Cold-Chain) | Not offered |
| Clinical Interpretation | Comprehensive report with ACGM guidelines & DHA-certified physician review | Basic variant list only |
Physician Insight & Safety Protocol
“As a physician, I understand that genetic testing for conditions like Fanconi anemia can be emotionally challenging. Please remember that a positive result does not guarantee disease onset, and a negative result does not eliminate all risk. Clinical correlation with hematology panels and family history remains essential.”
— Dr. PRABHAKAR REDDY, DHA License No. 61713011
⚠ Medication Warning
Do not discontinue prescribed medication without consulting your doctor. Genetic test results must be interpreted alongside your current treatment plan under medical supervision.
Exclusion Criteria & Emergency Red Flags
- This test is not suitable for individuals receiving a blood transfusion within the last two weeks, as donor DNA may interfere with genetic analysis.
- Not indicated for prenatal diagnosis without prior genetic counseling and informed consent.
- ER Red Flags: If you experience unexplained easy bruising, pallor, persistent fatigue, or recurrent infections, seek immediate medical attention regardless of test scheduling.
Patient FAQ & Clinical Guidance
Q1: What does the FANCE Gene NGS test detect?
Snippet: This test identifies pathogenic variants in the FANCE gene that cause Fanconi anemia type E and assess carrier status or future cancer risks.
Using a blood, extracted DNA, or one drop of blood on an FTA card, next-generation sequencing analyzes the entire coding region of the FANCE gene. The report indicates whether you carry one or two altered copies (carrier vs. affected) and details any known mutations linked to bone marrow failure, solid tumors, or leukemia predisposition. Results empower Hematologists, Oncologists, and Primary Care Doctors to tailor surveillance and early intervention.
ملخص الإجابة (بالعربية): يكشف هذا التحليل عن الطفرات الجينية المرضية في جين FANCE المسؤولة عن أنيميا فانكوني من النوع E، ويساعد في تقييم حالة الحامل للمرض ومخاطر السرطان المستقبلية، وذلك باستخدام تقنية تسلسل الجيل التالي (NGS) على عينة دم أو حمض نووي مستخلص.
Q2: How should I prepare for the test, and is there a specific diet or medication to stop?
Snippet: No fasting or dietary changes are required; continue prescribed medications and attend a pre‑test genetic counseling session to map your family pedigree.
Preparation is minimal. A healthcare professional will conduct a Genetic Counselling session to document a pedigree chart of family members affected by Fanconi anemia type E. This step is mandatory before sample collection and ensures the clinical context for accurate interpretation. Please do not alter any prescribed medications unless specifically instructed by your referring doctor.
ملخص الإجابة (بالعربية): لا يلزم الصيام أو تغيير النظام الغذائي؛ استمر في تناول أدويتك الموصوفة واحضر جلسة الاستشارة الوراثية لتخطيط شجرة العائلة قبل سحب العينة.
Q3: Will my insurance cover this, and how quickly can I receive my results?
Snippet: Direct billing to major UAE insurers is confirmed via WhatsApp at +971 54 548 8731, with results delivered within 3 to 4 weeks after sample receipt.
We support direct insurance verification for most local and international plans covering genetic testing for hereditary cancer syndromes. After approval, our VIP mobile phlebotomy team collects the sample from your home or office (8 AM – 11 PM). The laboratory processes the sample with ISO‑certified protocols, and your DHA‑licensed physician will provide a telephonic consultation to explain the findings once the report is ready.
ملخص الإجابة (بالعربية): يتم التحقق من تغطية التأمين مباشرة عبر واتساب رقم +971545488731، وتُصدر النتائج خلال 3 إلى 4 أسابيع بعد استلام العينة مع استشارة طبية هاتفية لتفسير التقرير.
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