Test Price
1,200 AED✅ Home Collection Available
JAK2 Mutation Detection Panel (Exon 12) in UAE | 1200 AED | 2026 DHA Guidelines
تحليل لوحة الكشف عن طفرات JAK2 (الإكسون 12) في الإمارات | 1200 درهم | معتمد من هيئة الصحة بدبي
Executive Summary | ملخص تنفيذي
دقة تشخيصية بنسبة 99.9% عبر معالجة معتمدة بأيزو 9001:2015. خدمة سحب منزلي من المستشفى بنظام التبريد المعتمد. إرشادات ما بعد الفحص عبر الهاتف. تحقق من التأمين مباشرة عبر واتساب +971 54 548 8731.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing.
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain and VIP Mobile Phlebotomy.
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Comprehensive Overview
The JAK2 Mutation Detection Panel (Exon 12) by Sanger sequencing is the gold standard for identifying rare pathogenic variants in the JAK2 gene, critical for diagnosing myeloproliferative neoplasms (MPNs). يُعد تحليل طفرات جاك 2 (الإكسون 12) الاختيار الأمثل للتشخيص الدقيق لأورام التكاثر النقوي.
| Feature | Our Test (ULAB) | Standard Alternative |
|---|---|---|
| Methodology | Sanger Sequencing (Gold Standard) | PCR-based Screening |
| Sensitivity | 99.9% for rare exon 12 mutations | Limited to common JAK2 V617F; may miss exon 12 variants |
| Turnaround Time | 7–8 Days | 5–7 Days |
| Cost | 1200 AED | ~900 AED (incomplete coverage) |
| Accreditation | ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139) | Varies |
Physician Insight & Safety Protocol
“As a clinician, I understand that genetic testing can be daunting. This targeted JAK2 exon 12 panel helps in refining diagnosis of myeloproliferative neoplasms, but results must be interpreted alongside complete blood counts and clinical history. Please do not discontinue any prescribed medication without consulting your doctor.” — Dr. Prabhakar Reddy, DHA License: 61713011
⚠️ Medication Warning:
Do not discontinue prescribed medication without consulting your doctor. Test results should never replace professional medical advice.
Exclusion Criteria & Emergency Red Flags:
- Not for minors (under 18) without legal guardian consent and prescription.
- Not applicable for surgery cases, pregnancy, or individuals planning international travel without a doctor’s prescription as per UAE regulations.
- If you experience symptoms such as sudden severe headache, vision changes, chest pain, or uncontrolled bleeding, seek immediate emergency care and inform the laboratory.
- Bone marrow aspiration carries inherent risks; proceed only if clinically indicated by a hematologist.
Patient FAQ & Clinical Guidance
1. What is the purpose of the JAK2 exon 12 mutation test?
Snippet: The JAK2 exon 12 mutation test identifies rare genetic variants in the JAK2 gene to aid diagnosis of polycythemia vera and other myeloproliferative neoplasms with high accuracy.
This test is specifically designed for patients with suspected MPN who test negative for the common JAK2 V617F mutation. It analyses exon 12 for clinically significant variants to confirm polycythemia vera or primary myelofibrosis, enabling targeted therapy and risk stratification.
2. ما هي مدة ظهور نتائج تحليل طفرات JAK2 (الإكسون 12)؟
خلاصة: تظهر نتائج تحليل طفرات JAK2 (الإكسون 12) خلال 7 إلى 8 أيام عمل باستخدام تقنية سانجر لتسلسل الحمض النووي، مما يضمن دقة عالية في الكشف.
يتم إرسال التقرير الرقمي مع استشارة هاتفية لتفسير النتائج من قبل أطبائنا المتخصصين فور الانتهاء من التحليل، مع إمكانية مناقشة النتائج مباشرة مع الطبيب المعالج.
3. Is fasting or special preparation required before the test?
Snippet: No fasting is needed, but a bone marrow or peripheral blood sample must be collected under strict clinical conditions with a doctor’s prescription mandatory.
For peripheral blood, standard venipuncture is used; for bone marrow, the procedure is performed by a specialist. Inform the phlebotomist of any anticoagulant therapy. The cannot be conducted for travel, surgery, or pregnancy without a valid prescription as per UAE Federal Decree-Law No. 41 of 2024.
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