Test Price
1,400 AED✅ Home Collection Available
RARA/PML Quantitative Test in UAE | 1400 AED | 2026 DHA Guidelines
تحليل RARA/PML الكمي في الإمارات | 1400 درهم | معتمد من هيئة الصحة بدبي
Executive Summary
✓ Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 accredited processing (cert. INT/EGQ/2509DA/3139).
✓ Premium Logistics: Paid hospital‑grade home collection with ISO‑certified cold‑chain transport. VIP mobile phlebotomy 8 AM–11 PM.
✓ Clinical Guidance: Telephonic post‑test result interpretation by a DHA‑licensed consultant.
✓ Insurance: Direct billing verification via WhatsApp +971 54 548 8731.
يقدم اختبار RARA/PML الكمي تشخيصًا جزيئيًا دقيقًا لابيضاض الدم الحادّ قليل التنسج (APL) عبر قياس نَسخة الاندماج PML-RARA بوساطة تفاعل البوليميراز المتسلسل الكمّي العكسي (RT-qPCR). يحقق دقة تصل إلى 99.9% في تحديد المرض وتقييم الحد الأدنى من المرض المتبقي، ما يُسهم في توجيه العلاج الكيميائي التفريقي. تُنفَّذ الفحوصات في مختبر معتمد وفقًا لمعايير DHA وتحت إشراف طاقم طبي متخصص.
RARA/PML Quantitative Test: What You Need to Know
The RARA/PML Quantitative Test is a highly sensitive molecular assay that detects the PML-RARA fusion gene, the definitive marker for acute promyelocytic leukemia (APL). This quantitative RT‑PCR assay measures the level of fusion transcript, essential for diagnosis, risk stratification, and minimal residual disease (MRD) monitoring.
| Feature | Our Test (RT-qPCR) | FISH (Qualitative) | Karyotyping |
|---|---|---|---|
| Method | Quantitative Reverse Transcription PCR | Fluorescence In Situ Hybridization | Chromosomal Banding Analysis |
| Sensitivity | >99% (1 leukemic cell in 105) | ~90% (requires ≥2% abnormal nuclei) | ~70–80% (only dividing cells) |
| Turnaround Time | 24‑72 hours | 2–4 days | 7–14 days |
| MRD Monitoring | Yes – quantitative | No | No |
Physician Insight & Safety Protocol
Dr. PRABHAKAR REDDY, Consultant Hematologist (DHA License: 61713011), advises: “A positive PML-RARA result must always be correlated with clinical presentation and complete blood counts. Never rely on a single test; treatment decisions for APL are urgent and require immediate haematologist consultation. This assay is a powerful monitoring tool for minimal residual disease, guiding early intervention.”
Critical Medication Warning
Do not discontinue any prescribed medication (including all‑trans retinoic acid, arsenic trioxide, or anticoagulants) without consulting your doctor.
Exclusion Criteria & Emergency Red Flags
- Not for routine screening – only for confirmed or highly suspected acute promyelocytic leukemia (APL) after haematologist referral.
- Minors require parental consent in accordance with UAE Child Protection Law (CDS 2026).
- If you experience sudden bleeding, persistent fever, severe fatigue, or confusion, seek emergency care immediately – do not wait for test results.
This service complies with Federal Decree‑Law No. 41 of 2024 (Art. 87) on medical liability and the UAE Personal Data Protection Law. All data handled with ISO‑certified confidentiality.
Patient FAQ & Clinical Guidance
What is the RARA/PML Quantitative Test?
This advanced molecular assay quantifies the PML-RARA fusion gene to diagnose acute promyelocytic leukemia and monitor minimal residual disease with 99.9% sensitivity. The test uses a small sample of blood or bone marrow to measure fusion transcript copy numbers through reverse transcription quantitative PCR (RT‑qPCR). It is the gold standard for confirming APL and tracking treatment response, often helping clinicians decide to modify or stop therapy as soon as the transcript becomes undetectable.
كم من الوقت يستغرق الحصول على نتائج الاختبار؟
تُصدر النتائج النهائية عبر البريد الإلكتروني خلال 3 أيام عمل (36 ساعة)، مع إمكانية إخطار هاتفي عاجل في غضون 24 ساعة. نقدم خدمة إبلاغ سريعة للحالات الإسعافية عبر الهاتف، ويُتبع ذلك تقرير مفصّل يُرسل إلى بريدك الإلكتروني مباشرة. يضمن نظام السلسلة الباردة المعتمد سلامة العينة ودقة النتائج طيلة عملية النقل والتحليل.
How should I prepare for the and what sample is required?
You need to sign a consent document and bring your complete clinical history, including any prior leukemia treatment records. The sample is collected by a trained phlebotomist – usually a peripheral blood draw, or in certain cases a bone marrow aspiration performed by a haematologist. Our home collection team adheres to strict cold‑chain protocols to preserve RNA integrity. Please inform us of any blood‑thinning medications beforehand. Results are interpreted by a DHA‑licensed specialist and shared with you securely.
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8 AM – 11 PM | 1400 AED | DHA‑Compliant
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