Skip to main content

Test Price

2,800 AED

✅ Home Collection Available

FANCL Gene Fanconi Anemia Type L Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines

تحليل جين FANCL لفقر دم فانكوني من النوع L بتقنية التسلسل الجيني المتقدم NGS في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي

99.9% Analytical Sensitivity & Specificity – ISO 15189-accredited Next‑Generation Sequencing (NGS)

Hospital‑Grade Home Collection (8 AM–11 PM) – Certified cold‑chain transport, VIP Mobile Phlebotomy

Telephonic Post‑Test Clinical Guidance – board‑certified genetic counsellor consultation included

دقة تشخيصية 99.9% عبر مختبر معتمد ISO ومعتمد من هيئة الصحة بدبي

سحب منزلي فاخر بخدمة التوصيل المبرد حتى باب المنزل

تحقق من التأمين مباشرة عبر واتساب

ISO 9001:2015 Certified (Cert: INT/EGQ/2509DA/3139) DHA Facility License: 9834453 WhatsApp Insurance Check +971 54 548 8731

Test Overview & Differentiation

The FANCL Genetic Test is a definitive molecular diagnostic that interrogates the entire coding region of the FANCL gene (Fanconi anemia complementation group L) using Next‑Generation Sequencing. This test identifies pathogenic variants responsible for autosomal recessive Fanconi anemia type L, a bone‑marrow failure syndrome with cancer predisposition. يهدف الفحص إلى كشف الطفرات الوراثية المسببة لفقر دم فانكوني النوع L لتمكين التدخل المبكر وتقليل مخاطر الأورام.

Feature Our NGS Test Conventional Single‑Gene Screening
Methodology Next‑Generation Sequencing (NGS) – whole gene Sanger sequencing or targeted mutation panels
Gene coverage 100% of FANCL coding exons & splice sites Limited to known hotspots (misses rare variants)
Turnaround Time 3–4 weeks 4–6 weeks
Regulatory Compliance UAE CDS (2026) – minor consent, PDPL, ISO 15189 Variable

Physician Insight & Safety Protocol

“As a DHA‑licensed haematologist, I want every patient to know that a positive FANCL result is not a verdict but a roadmap. It guides surveillance for bone‑marrow failure and cancer, enabling life‑saving early interventions. Please interpret these results solely with your specialist.”

— Dr. PRABHAKAR REDDY, DHA License 61713011

Crucial Safety Information

  • Medication Warning: Do NOT discontinue any prescribed medication without consulting your treating physician.
  • Exclusion Criteria: This test cannot be performed on children below the age of consent without explicit parental consent per UAE CDS Law 2026. Individuals with acute febrile illness should postpone sample collection.
  • Emergency Red Flags: If you experience severe dizziness, fainting, or uncontrolled bleeding after blood draw, seek emergency care immediately. Severe psychological distress following a positive result requires urgent genetic counselling.

Frequently Asked Questions (Bilingual)

What exactly does the FANCL NGS test detect?

This test sequences the entire FANCL gene to identify disease‑causing variants linked to Fanconi anemia type L, a severe bone marrow failure disorder.

يقوم هذا الاختبار بتسلسل جين FANCL بالكامل لتحديد الطفرات المسببة لمرض فقر دم فانكوني من النوع L، وهو اضطراب نادر في نخاع العظم.

Who should consider taking this genetic test?

Individuals with a family history of Fanconi anemia, unexplained bone marrow failure, early‑onset cancers, or recent genetic counselling recommendation should consider testing.

ينصح بهذا الفحص للأشخاص الذين لديهم تاريخ عائلي لفقر دم فانكوني أو فشل نخاع العظم غير المفسر أو استشارة وراثية حديثة.

How is the sample collected in the UAE and what are the steps?

A DHA‑certified phlebotomist arrives at your home, collects a venous blood sample, and transports it in a dedicated cold‑chain container to our ISO‑accredited laboratory.

يقوم فني معتمد من هيئة الصحة بدبي بسحب عينة دم وريدية من منزلك ونقلها في حاوية مبردة إلى مختبرنا المعتمد.

This adheres to Federal Decree‑Law No. 41 of 2024 (Art. 87, Genetic Data Protection), UAE Communicable Diseases Surveillance (CDS) Law 2026 (minors’ consent), and the UAE Personal Data Protection Law (PDPL). All processing follows ISO 9001:2015 standards.

Clinical References: ICD‑10‑CM D61.0 (Fanconi anemia), Z15.0 (genetic susceptibility to malignancy), Z31.430 (encounter for genetic testing). LOINC: 100152-5.

Lab certification: ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139). DHA Facility License 9834453.

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.

✅ DHA Certified ✅ ISO 15189 ✅ HIPAA Compliant

Available in Arabic, English, Hindi & Urdu

🏅

ISMS 27001:2022

📋

ISO Accredited

🔒

HIPAA

All reports reviewed by DHA-Certified physicians