Test Price
2,800 AED✅ Home Collection Available
Factor XI Deficiency (F11) Gene Sequencing Test (NGS) in UAE | 2800 AED | 2026 DHA Guidelines
اختبار جين F11 لنقص العامل الحادي عشر في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
✓ Diagnostic Accuracy Guarantee: 99.9% analytical sensitivity and specificity for F11 gene variant detection via ISO 9001:2015 accredited NGS platform.
✓ Premium Home Collection: Complimentary hospital-grade, cold-chain home sample collection by DHA-licensed phlebotomists, 8 AM – 11 PM.
✓ Post-Test Clinical Guidance: Telephonic result interpretation by a genetic counselor, ensuring actionable clinical insights.
✓ Insurance Support: Direct billing verification via WhatsApp at +971 54 548 8731.
نضمن دقة التشخيص بنسبة 99.9% عبر مختبراتنا المعتمدة وفق معايير ISO 9001:2015 وتحت إشراف هيئة الصحة بدبي.
- Sample: Blood (EDTA), Extracted DNA, or One-drop Blood on FTA Card
- Methodology: Next-Generation Sequencing (NGS)
- License: 9834453 (DHA/MOHAP)
- ISO: 9001:2015 (Cert: INT/EGQ/2509DA/3139)
Test Overview & Why It Matters
This NGS-based genetic test fully sequences the F11 gene to identify pathogenic variants responsible for hereditary factor XI deficiency, a rare bleeding disorder primarily characterized by prolonged bleeding after trauma or surgery. يستخدم هذا الفحص تقنية التسلسل الجيني المتقدم لتحديد الطفرات المسببة لنقص العامل الحادي عشر، مما يساعد في التشخيص المبكر وتقييم مخاطر النزيف العائلي.
| Feature | Our Test (F11 NGS) | Closest Alternative |
|---|---|---|
| Precision | 99.9% analytical sensitivity/specificity | Sanger sequencing (~99%)—limited to coding regions only |
| Method | Full gene NGS (all exons, splice sites) | Targeted mutation panel or single‑exon Sanger |
| Turnaround | 3–4 weeks | 2–4 weeks (often requires multiple rounds) |
Physician Insight & Safety Protocol
“A F11 deficiency diagnosis must always be correlated with personal and family bleeding histories. One mutation may cause mild bleeding in some individuals and significant surgical bleeding in others; genetic results alone do not predict severity. Please engage your hematologist to integrate these findings into a tailored management plan.”
— Dr. PRABHAKAR REDDY, DHA License 61713011
⚠ Medication Safety Warning
Do not discontinue or alter any prescribed medication without consulting your physician. Certain blood‑thinning agents (e.g., warfarin, DOACs) require careful management around genetic testing and procedural planning.
Exclusion Criteria & Emergency Red Flags
- Exclusion: Active, uncontrolled bleeding; inability to provide informed consent; pregnancy (relative; requires specialist clearance).
- Seek urgent medical attention if you experience: sudden severe bleeding, blood in urine or stool, prolonged nosebleeds (>20 min), signs of intracranial bleeding (severe headache, vision changes, confusion).
Frequently Asked Questions
1. What does the F11 gene test detect?
Snippet Answer: This test analyzes the entire F11 gene using Next‑Generation Sequencing to identify mutations causing hereditary factor XI deficiency.
The analysis covers all coding exons and adjacent splice junctions. Results are interpreted according to current ACMG guidelines and reported with clinical significance (pathogenic, likely pathogenic, VUS). A negative result does not exclude the presence of deep intronic variants or deletions/duplications that may require additional testing.
ما الذي يكشفه اختبار جين F11؟
يكشف هذا الاختبار الطفرات الوراثية في جين F11 المرتبطة بنقص العامل الحادي عشر، مما يساعد في التشخيص وتقييم المخاطر لدى العائلة.
2. How should I prepare for the test?
Snippet Answer: A pre‑ genetic counseling session is mandatory to draw a pedigree chart and discuss the implications of the results.
No fasting is required for blood collection. If you are on anticoagulants, inform our team during scheduling. For FTA card samples, a single drop of blood is adequate. All samples are transported under strict cold‑chain (2‑8°C) to maintain DNA integrity.
كيف أستعد للاختبار؟
يلزم جلسة استشارة وراثية قبل الاختبار لرسم شجرة العائلة ومناقشة النتائج المحتملة، ولا يشترط الصيام.
3. Are results confidential and compliant with UAE law?
Snippet Answer: All genetic data is protected under UAE PDPL, processed inside DHA‑licensed facilities, and never shared without explicit written consent.
The laboratory adheres to Federal Decree‑Law No. 41 of 2024 and the 2026 CDS Law for minors. Results are delivered exclusively to the ordering physician or directly to the patient through secure encrypted channels. No information is disclosed to insurers or third parties without authorization.
هل النتائج سرية ومتوافقة مع قوانين الإمارات؟
تحمى البيانات الجينية بموجب قانون حماية البيانات الشخصية الإماراتي (PDPL) ولا تُشارك إلا بموافقة خطية صريحة من المريض.
UAE Legal Compliance & E‑E‑A‑T
This service is operated under DHA Facility License 9834453 and complies with Federal Decree‑Law No. 41 of 2024 (Art. 87) and the 2026 CDS Law for Minors. All personal genetic data is protected following UAE PDPL. ISO 9001:2015 certification (Cert: INT/EGQ/2509DA/3139) guarantees quality management across all pre‑analytical, analytical and post‑analytical phases.
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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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