Test Price
2,000 AED✅ Home Collection Available
ALL FISH Panel (Acute Lymphoblastic Leukemia) in UAE | 2000 AED | 2026 DHA Guidelines
تحليل لوحة FISH لابيضاض الدم الليمفاوي الحاد (ALL) في الإمارات | 2000 درهم | معتمد من هيئة الصحة بدبي
Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing.
Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection & VIP Mobile Phlebotomy.
Clinical Guidance: Telephonic Post-Test Clinical Guidance in Result Interpretation provided by a Specialist Team.
Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
الخلاصة التنفيذية: نضمن دقة تشخيصية تصل إلى 99.9% عبر معالجة معتمدة بموجب ISO 9001:2015. نقدم خدمات متميزة تشمل جمع العينات منزلياً تحت ظروف سلسلة التبريد المعتمدة وخبرة السحب الفموي المتنقل. كما نوفر إرشاداً طبياً بعد الفحص عبر الهاتف لدعم تفسير النتائج، مع إمكانية التحقق المباشر من التغطية التأمينية عبر واتساب.
Comprehensive Genetic Profiling for Leukemia
The ALL FISH Panel is a targeted molecular cytogenetic test that detects four critical chromosomal rearrangements (BCR::ABL1, ETV6::RUNX1, KMT2A, and TCF3) in patients with suspected or confirmed acute lymphoblastic leukemia, guiding precise diagnosis, risk stratification, and therapy selection. تقدم هذه اللوحة تشخيصاً دقيقاً وسريعاً لابيضاض الدم الليمفاوي الحاد باستخدام تقنية التهجين الموضعي المتألق (FISH).
| Feature | Our ALL FISH Panel | Conventional Karyotyping |
|---|---|---|
| Precision & Resolution | Sub‑microscopic rearrangements; >99% analytical sensitivity | Limited to >5 Mb aberrations; requires dividing cells |
| Methodology | Interphase Fluorescence In‑Situ Hybridization (FISH) | Giemsa‑banding chromosome analysis |
| Turnaround Time | 10 calendar days | 14–21 days (culture‑dependent) |
| Clinical Utility | Definitive risk‑group assignment; MRD monitoring | Genome‑wide screen; lower resolution |
*Comparison based on 2026 DHA‑endorsed laboratory standards.
Physician Insight & Safety Protocol
“As a clinician, I recognize that the ALL FISH Panel provides invaluable molecular markers, but it must always be correlated with the full clinical picture, morphology, and immunophenotype. Never alter treatment without a comprehensive multidisciplinary review. — Dr. PRABHAKAR REDDY (DHA License: 61713011)”
⚠ Medication Warning: Do not discontinue prescribed medication or modify your treatment plan without consulting your treating physician.
Safety & Appropriateness
- Exclusion Criteria: This test is not indicated for asymptomatic individuals or general health screening. It is intended only for patients with a clinical suspicion or confirmed diagnosis of acute leukemia. Sample collection is not performed on patients with active severe coagulopathy unless corrected.
- Emergency Red Flags: If you experience sudden high fever with rigors, uncontrolled bleeding, new neurological symptoms, or severe shortness of breath, seek immediate emergency care and inform the ER team that you are undergoing leukemia evaluation.
Required Prescription & Sample Logistics
- A valid physician’s prescription is required for this panel. Exceptions: surgical clearance mandated by a hospital, pregnancy‑related emergencies, and pre‑travel regulatory medical reports – in these cases appropriate statutory documentation may replace the prescription.
- Sample type: Bone marrow aspirate (preferred) or peripheral blood. Specimen must be collected in a heparinised syringe (bone marrow) or EDTA tube (peripheral blood) and transported immediately at room temperature. Delayed transport beyond 2 hours may compromise cell viability and result accuracy.
- No fasting or medication avoidance is required solely for the FISH procedure, but follow your doctor’s specific preparation instructions.
Frequently Asked Questions
1. Why is the ALL FISH Panel important for my diagnosis?
Snippet: This panel identifies four key chromosomal translocations that classify acute lymphoblastic leukemia into risk groups and guide precise therapy.
The ALL FISH Panel detects BCR::ABL1, ETV6::RUNX1, KMT2A, and TCF3 rearrangements, each with distinct prognostic significance. For example, ETV6::RUNX1 typically indicates a favourable outcome in children, while KMT2A rearrangement confers high risk. The results help your haematologist‑oncologist choose the most effective chemotherapy or targeted agent.
الإجابة المختصرة: تكشف هذه اللوحة أربعة تحولات كروموسومية رئيسية تصنف ابيضاض الدم الليمفاوي الحاد إلى مجموعات خطورة وتوجه العلاج الدقيق.
2. Can this be performed on a simple blood draw instead of bone marrow?
Snippet: While peripheral blood can be used when circulating blasts are high, bone marrow aspirate remains the gold standard for diagnostic accuracy.
In many cases of ALL, leukaemic cells spill into the bloodstream, allowing FISH analysis on peripheral blood. However, if the percentage of abnormal cells is low, a bone marrow sample yields more reliable results. Your physician will determine the most appropriate sample type based on your complete blood count and blast percentage.
الإجابة المختصرة: يمكن استخدام الدم المحيطي عند وجود أرومات مرتفعة، لكن نخاع العظم يظل المعيار الذهبي للتشخيص الدقيق.
3. How soon will I receive my results and who interprets them?
Snippet: The standard turnaround time is 10 working days, and a board‑certified molecular pathologist provides the final signed report with interpretive comments.
Our laboratory adheres to strict quality controls with dual‑review of FISH signals. Once the report is issued, you will have access to a telephonic consultation where a clinical specialist explains the findings in the context of your overall diagnosis. All reports are transmitted securely via encrypted email or the patient portal.
الإجابة المختصرة: تصدر النتائج خلال 10 أيام عمل، ويقدمها أخصائي علم الأمراض الجزيئي مع شروحات تفسيرية.
This service complies with Federal Decree-Law No. 41 of 2024 (Art. 87) on medical advertising, the UAE Patient Data Privacy Law (PDPL), and the 2026 Child Data Sovereignty (CDS) Law requiring explicit parental consent for minors. All processing is performed under ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139) accredited laboratory standards. For insurance pre‑authorisation or appointment scheduling, contact +971 54 548 8731 (WhatsApp available).
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التحقق من التغطية التأمينية
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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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