Test Price
2,800 AED✅ Home Collection Available
FAS Gene Autoimmune Lymphoproliferative Syndrome Type 1A (ALPS) Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين FAS لمتلازمة التكاثر اللمفاوي المناعي الذاتي من النوع 1A في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
🔬 Diagnostic Accuracy Guarantee
99.9% diagnostic sensitivity and >99.99% analytical specificity via ISO 9001:2015 certified NGS (Cert: INT/EGQ/2509DA/3139).
🏥 Premium Home Collection
Hospital‑grade, cold‑chain logistics with VIP mobile phlebotomy, available daily 8 AM – 11 PM.
📋 Post‑Test Clinical Guidance
Complimentary telephonic interpretation session with a DHA‑licensed genetic counsellor.
💳 Insurance Support
Direct billing verification via WhatsApp at +971 54 548 8731; most major UAE insurers accepted.
📌 الملخص التنفيذي
يضمن تسلسل الجيل التالي (NGS) لجين FAS دقة تشخيصية بنسبة 99.9% تحت إشراف هيئة الصحة بدبي ووفقًا للمرسوم الاتحادي رقم 41 لسنة 2024. تُجرى سحب العينات بطريقة معقمة فائقة في منزلك مع نقل مبرد، يليها تقرير مفصل وجلسة إرشاد وراثي. السعر 2800 درهم – يُدفع مباشرة أو عبر التأمين. للاستفسار: واتساب +971545488731.
Comprehensive Genetic Analysis for Autoimmune Lymphoproliferative Syndrome
This next‑generation sequencing test interrogates the entire coding region of the FAS gene to confirm clinical diagnosis of autoimmune lymphoproliferative syndrome type 1A, enabling precise risk stratification and tailored management. يستخدم هذا الفحص تقنية التسلسل الجيني لتحليل جين FAS بالكامل وتأكيد تشخيص المتلازمة اللمفاوية المناعية الذاتية من النوع 1A.
| Feature | Our Test (NGS Full Gene Sequencing) | Targeted Mutation Panel (Reference Lab) |
|---|---|---|
| Methodology | Next‑Generation Sequencing (Illumina® platform, 100x mean depth) | Sanger sequencing of 3‑5 hotspots only |
| Analytical Sensitivity | >99.99% (single nucleotide variants & small indels) | ~85‑90% (misses deep intronic/novel variants) |
| Turnaround Time | 3‑4 weeks | 2‑3 weeks |
| Clinical Utility | Confirms diagnosis, familial cascade testing, lymphoma risk | Preliminary screening only |
🩺 Physician Insight & Safety Protocol
“This test must always be interpreted in the context of your complete clinical picture and family history. A negative result does not exclude all immune dysregulation disorders, and a variant of uncertain significance warrants further family studies. Your referring immunologist or rheumatologist will guide you through the post‑test implications.”
— Dr. Prabhakar Reddy, DHA‑licensed Clinical Geneticist (License #61713011)
Do not discontinue or modify any prescribed medication without consulting your treating physician.
🚫 Exclusion Criteria & ER Red Flags
- Exclusion: Asymptomatic minors without parental consent, or individuals who have not undergone pre‑test genetic counselling.
- Exclusion: Patients with known bone marrow failure not suspected of ALPS (requires separate workup).
- Red Flag: Sudden massive lymphadenopathy, progressive pancytopenia, or night sweats – seek emergency haematology evaluation immediately.
- Red Flag: Rapid splenomegaly with unexplained bruising or bleeding may indicate aggressive lymphoma requiring urgent imaging.
❓ Patient FAQ & Clinical Guidance
1. What is the purpose of this genetic test?
This test detects FAS gene mutations linked to autoimmune lymphoproliferative syndrome type 1A, confirming diagnosis and informing treatment. يحدد هذا الفحص الطفرات في جين FAS المسؤول عن متلازمة التكاثر اللمفاوي المناعي الذاتي من النوع 1A، مما يساعد في التشخيص ووضع خطة العلاج.
2. How should I prepare for the test?
Provide a detailed clinical history and attend a pre‑test genetic counselling session to map your family pedigree. قدِّم تاريخًا طبيًا مفصلاً واحضر جلسة استشارة وراثية قبل الاختبار لرسم شجرة العائلة.
3. How long will results take and what should I do next?
Results are available in 3-4 weeks; a telephonic counselling session will explain findings and next clinical steps. تظهر النتائج خلال 3 إلى 4 أسابيع، تليها جلسة استشارة هاتفية لشرح النتائج والإرشادات السريرية التالية.
📄 Pre‑ Requirements
A comprehensive clinical history including previous immunological workups is mandatory. All patients must undergo a formal genetic counselling session (by a DHA‑licensed professional) to draw the family pedigree and obtain informed consent prior to sample collection.
🩸 Accepted Sample Types
- Whole blood (2‑5 mL in EDTA tube)
- Extracted DNA (minimum 1 µg, A260/280 ratio 1.8‑2.0)
- One drop of blood on FTA card (dried blood spot)
Facility License: 9834453 | ISO 9001:2015 Certified (Cert: INT/EGQ/2509DA/3139) | UAE PDPL & Federal Decree-Law No. 41/2024 Art. 87 compliant.
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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