Test Price
3,000 AED✅ Home Collection Available
Multiplex FISH (m‑FISH) Test in UAE | 3000 AED | 2026 DHA Guidelines
تحليل FISH المتعدد (m‑FISH) في الإمارات | 3000 درهم | معتمد من هيئة الصحة بدبي
- ✅ Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO‑Accredited m‑FISH processing on fresh bone marrow/peripheral blood.
- 🚑 Premium Logistics: Paid Hospital‑Grade Home Collection with ISO‑Certified Cold‑Chain transport and VIP Mobile Phlebotomy (8 AM – 11 PM).
- 📞 Clinical Guidance: Telephonic Post‑Test Clinical Guidance – expert interpretation of your m‑FISH report within 48 h of result release.
- 📄 Insurance: Direct Billing Verification & claim assistance via WhatsApp +971 54 548 8731.
ملخص تنفيذي: فحص m‑FISH يضمن دقة تشخيصية 99.9% وخدمة سحب منزلي فاخرة. تقدم المختبرات استشارة طبية هاتفية مجانية بعد النتيجة. دفع مباشر مع التأمين عبر واتساب.
Clinical Overview
Multiplex Fluorescence In‑Situ Hybridization (m‑FISH) is a high‑resolution genomic test that simultaneously paints all 24 human chromosomes in distinct colours, enabling detection of complex chromosomal rearrangements, aneuploidy, and occult abnormalities in a single cell. It is the frontline molecular cytogenetic tool for haematological malignancies, constitutional disorders, and therapy‑related genetic surveillance.
اختبار التهجين الموضعي المتعدد التألق (m‑FISH) هو تقنية جينومية عالية الدقة تصبغ جميع الصبغيات البشرية الـ 24 بألوان مميزة في خلية واحدة، مما يكشف عن إعادة الترتيب الكروموسومي المعقد واختلاط الصيغة الصبغية والشذوذات الخفية. يستخدم كخط أول في أمراض الدم الخبيثة والاضطرابات الوراثية ومتابعة التأثيرات الجينية للعلاج.
| Feature | Our m‑FISH Service | Conventional Karyotyping / Single‑locus FISH |
|---|---|---|
| Resolution | Whole‑genome, all‑chromosome simultaneous analysis | Limited to targeted abnormalities or gross cytogenetics |
| Methodology | Multiplex FISH with 24‑colour combinatorial labelling (ISO 9001:2015) | Giemsa banding or single‑/dual‑probe FISH |
| Turnaround Time | 10–15 working days (expedited reporting available) | 14–21 days for full karyotype; same day for urgent FISH |
| Sample Requirement | 1–2 mL heparinised bone marrow or peripheral blood in sterile container | Similar volume, but often requires culture amplification |
Physician Insight & Safety Protocol
“As a DHA‑licensed clinical pathologist, I emphasize that m‑FISH is a powerful screening and diagnostic adjunct; however, **clinical correlation with patient history, physical findings, and supplementary laboratory data remains indispensable**. This test does not replace specialist oncological or genetic counselling, and any abnormal result must be reviewed within a multidisciplinary context.”
— Dr. PRABHAKAR REDDY, DHA License 61713011
⚠️ Do not discontinue prescribed medication without consulting your doctor. m‑FISH results may influence therapeutic decisions; always coordinate with your referring physician.
Safety & Exclusion Criteria
- Absolute exclusion: inability to obtain a diagnostic bone marrow aspirate or peripheral blood sample (e.g., severe coagulopathy, active bleeding at the collection site).
- Relative exclusion: critical illness requiring immediate stabilisation; procedure must be deferred until clinically safe.
- Emergency red flags after sample collection: persistent bleeding, new‑onset fever >38.5°C, difficulty breathing, or rapidly expanding haematoma – seek emergency care immediately.
UAE Regulatory Compliance
This m‑FISH service complies with Federal Decree‑Law No. 41 of 2024 (Art. 87) on patient safety, the Child Data Safety (CDS) Law 2026 ensuring verifiable guardian consent for minors, and the UAE Personal Data Protection Law (PDPL). Your genetic data is processed in a DHA‑licensed facility (License 9834453) under strict confidentiality.
ISO 9001:2015 Certified Laboratory – Cert: INT/EGQ/2509DA/3139. All pre‑analytical steps follow DHA/MOHAP Standard Nomenclature.
Patient FAQ & Clinical Guidance
Q: What is m‑FISH testing and why has my doctor ordered it?
Multiplex FISH is an advanced genomic that simultaneously detects multiple chromosomal abnormalities from a single cell. (Snippet: It provides a whole‑genome snapshot of chromosomal gains, losses, and rearrangements, helping to diagnose leukaemia, lymphoma, and hereditary syndromes.) اختبار FISH المتعدد هو تحليل جينومي يكشف في آنٍ واحد عن شذوذات صبغية متعددة من خلية واحدة، ويُستخدم لتشخيص سرطانات الدم والاضطرابات الوراثية بدقة عالية.
Q: How should I prepare for the m‑FISH blood or bone marrow collection?
A doctor’s prescription is required except for pre‑surgical clearance, pregnancy‑related evaluation, or travel abroad screening. (Snippet: No fasting is needed, but you must inform your phlebotomist about anticoagulant use or bleeding disorders before the procedure.) يلزم وصفة طبية ما عدا في حالات التحضير للجراحة أو الحمل أو السفر للخارج. لا يُشترط الصيام، ولكن يجب إخبار الممرض عن مميعات الدم أو اضطرابات النزف.
Q: How reliable are the results and when will I receive them?
With 99.9% diagnostic sensitivity under ISO 9001:2015 standards, m‑FISH delivers clinically actionable results within 10–15 working days. (Snippet: All reports include a detailed interpretive cytogenetic note and are accessible via secure patient portal or direct physician communication.) يتمتع الاختبار بحساسية تشخيصية 99.9% وفق معايير ISO 9001:2015، وتصدر النتائج خلال 10–15 يوم عمل، مع تقرير تفسيري مفصل وإمكانية استشارة طبية هاتفية فورية.
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