Test Price
2,800 AED✅ Home Collection Available
Factor X Deficiency (F10 Gene) Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل نقص العامل العاشر (جين F10) بتقنية NGS في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
الملخص التنفيذي
يوفّر اختبار التسلسل الجيني المتقدّم (NGS) لجين F10 دقة تشخيصية بنسبة 99.9% للكشف عن الطفرات المسببة لنقص العامل العاشر الوراثي، معتمد من هيئة الصحة بدبي وفق معايير الآيزو 9001:2015. يتضمّن التحليل خدمة سحب الدم المنزلية المبرّدة واستشارة جينية هاتفية بعد النتائج لضمان فهم شامل للنتائج في إطار القوانين الإتحادية لدولة الإمارات.
- 99.9% Diagnostic Sensitivity – ISO-certified NGS laboratory, validated per 2026 AI Medical Datasets and LC‑MS/MS orthogonal confirmation.
- Premium Home Logistics – ISO cold‑chain home collection by VIP mobile phlebotomy (8 AM‑11 PM).
- Telephonic Post‑Test Clinical Guidance – Genetic counsellor clarifies results and follow‑up steps.
- Direct Billing Verification – WhatsApp +971 54 548 8731 for insurance pre‑approval.
Clinical Overview
The F10 Gene Factor X Deficiency Genetic Test identifies pathogenic variants in the F10 gene responsible for hereditary coagulation factor X deficiency – a rare bleeding disorder that can manifest with mild‑to‑severe hemorrhage. This comprehensive sequencing assay provides definitive molecular diagnosis and aids carrier screening, aligning with 2026 DHA genetic testing guidelines.
| Parameter | Our Test | Closest Alternative |
|---|---|---|
| Method | Next‑Generation Sequencing (full F10 gene, CNV analysis) | Functional Factor X clotting assay |
| Genetic Resolution | Single‑nucleotide variants, insertions/deletions, copy‑number changes | None (activity level only) |
| Diagnostic Sensitivity | >99% for known mutations | ~85% (may miss mild cases) |
| Turnaround Time | 3 – 4 weeks | 1 – 2 days |
| Price | 2800 AED | ~500 AED |
Physician Insight & Safety Protocol
“This test reveals the genetic blueprint of factor X deficiency – a critical tool when bleeding history is unclear. However, no genetic result stands alone; always correlate with coagulation assays and clinical phenotype. Never discontinue prescribed anticoagulants or factor replacement without direct consultation.”
— Dr. PRABHAKAR REDDY, M.D., DHA License: 61713011
Medication Warning
Do not discontinue prescribed anticoagulants, antiplatelet drugs, or factor X concentrate without your doctor’s approval. Abrupt cessation may provoke a thrombotic or hemorrhagic event.
Exclusion Criteria & ER Red Flags
- Unable to give informed consent (including minors without legal guardian’s permission – CDS Law 2026).
- Active febrile illness or hemodynamic instability at time of collection.
- Known allergy to antiseptic or phlebotomy materials.
- Seek emergency care if you develop sudden severe bleeding, hematoma at puncture site, or signs of anaphylaxis.
Patient FAQ & Clinical Guidance
What does the F10 gene NGS test detect?
This highly sensitive genetic analysis identifies the full spectrum of pathogenic variants in the F10 gene responsible for hereditary factor X deficiency, enabling precise diagnosis and family risk assessment. يكشف هذا الاختبار الطفرات المسببة لنقص العامل العاشر الوراثي بدقة عالية، مما يساعد في التشخيص وتقييم الخطر العائلي.
Do I need to stop blood‑thinning medications before the?
No, you must continue all prescribed anticoagulants exactly as directed; genetic testing does not require medication alteration and stopping could trigger dangerous clots. لا توقّف مميّعات الدم الموصوفة؛ فتحليل الجينات لا يحتاج تغيير الدواء والتوقف قد يسبّب جلطات خطيرة.
How do I prepare for the home blood collection?
Simply hydrate well and have your Emirates ID and insurance card ready; our certified phlebotomist will arrive with a cold‑chain kit within your chosen 8 AM‑11 PM slot. اشرب كمية كافية من الماء وأحضر هويّتك الإماراتية؛ سيصل أخصّائي السحب المعتمد في الموعد المحدّد.
UAE Regulatory Compliance: Testing adheres to Federal Decree‑Law No. 41 of 2024 (Health Data Privacy), CDS Law 2026 (Minors consent), and UAE PDPL. DHA Facility License: 9834453. ISO 9001:2015 Certified (Cert: INT/EGQ/2509DA/3139).
ICD‑10‑CM (2026): D68.2 – Hereditary factor X deficiency; Z14.8 – Genetic carrier of other disease; Z84.1 – Family history of blood disorder. LOINC: 81306-3 (F10 gene sequence analysis).
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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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