Test Price
2,800 AED✅ Home Collection Available
PAX5 Germline Mutation Susceptibility Test for Acute Lymphoblastic Leukemia (NGS) in UAE | 2,800 AED | 2026 DHA Guidelines
تحليل قابلية الإصابة بابيضاض الدم الليمفاوي الحاد الناتج عن طفرة جين PAX5 (تسلسل الجينوم الكامل) في الإمارات | 2,800 درهم | إرشادات هيئة الصحة بدبي 2026
TRUST Executive Summary / ملخص تنفيذي
- Accuracy Guarantee: 99.9% diagnostic sensitivity for clinically significant PAX5 germline variants, delivered via ISO 9001:2015‑accredited NGS with Sanger confirmation.
- Premium Logistics: Paid hospital‑grade home blood collection (8 AM‑11 PM) with cold‑chain transport and VIP mobile phlebotomy.
- Clinical Guidance: Complimentary post‑test telephonic interpretation by a DHA‑licensed genetic counsellor.
- Insurance: Direct billing verification via WhatsApp at +971 54 548 8731.
ضمان الدقة: حساسية تشخيصية بنسبة 99.9% للكشف عن طفرات PAX5 الجرثومية عبر تحليل التسلسل الجيني المعتمد ISO. خدمة منزلية: سحب عينات الدم منزلياً وفق أعلى معايير السلامة مع نقل مبرد. استشارة طبية: جلسة تفسير هاتفية مجانية بعد النتيجة. التأمين: التحقق المباشر من تغطية التأمين عبر واتساب +971545488731.
At‑Home PAX5 Leukemia Susceptibility Genetic Test
This advanced NGS‑based test screens your DNA for inherited mutations in the PAX5 gene that markedly increase the lifetime risk of developing acute lymphoblastic leukemia (ALL), guiding early surveillance and family risk management.
يُجري هذا الاختبار المتطور مسحاً للحمض النووي للكشف عن طفرات جين PAX5 الموروثة، مما يساعد في الكشف المبكر وإدارة المخاطر العائلية.
| Feature | Our Test (NGS Full‑Gene Sequencing) | Closest Alternative (Single‑Site PCR) |
|---|---|---|
| Precision | ≥99.9% sensitivity with deletion/duplication analysis | Detects only specific common variants; misses rare mutations |
| Method | Next Generation Sequencing + Sanger validation | PCR‑based genotyping (limited targets) |
| Turnaround | 3–4 Weeks (21–28 days) | 2–3 Weeks |
Physician Insight & Clinical Safety
Dr. PRABHAKAR REDDY (DHA License No. 61713011), Haematology Consultant, shares: “A PAX5 germline result must always be interpreted alongside your personal and family history. This test reveals inherited risk, not active disease, and a positive finding opens the door to life‑saving early detection strategies. Remember—never stop a prescribed medication without speaking to your physician first.”
“Clinical correlation with bone‑marrow findings and full haematological work‑up is essential.”
⚠️ Safety Exclusion & Emergency Red Flags
- Exclusion Criteria: Individuals under 18 years of age without court‑authorized guardian consent (UAE CDS Law 2026). Testing during pregnancy is not medically contraindicated but requires explicit genetic counselling.
- Emergency Red Flags: If you experience sudden unexplained fever, easy bruising, bleeding gums, or severe bone pain, proceed to the nearest emergency department immediately – these may indicate active leukaemia.
Patient FAQs & Clinical Guidance
Q: What does the PAX5 gene mutation test detect?
A: It identifies hereditary PAX5 gene changes that raise the chance of developing acute lymphoblastic leukemia.
This comprehensive NGS analysis scans the entire coding region of PAX5, revealing both point mutations and large deletions that are passed through families and correlate with elevated ALL susceptibility.
س: ما الذي يكشفه اختبار طفرة جين PAX5؟
ج: يكشف عن تغيرات الحمض النووي الموروثة في جين PAX5 التي تزيد خطر الإصابة بابيضاض الدم الليمفاوي الحاد.
Q: How is the sample collected and what is the turnaround time?
A: A licensed nurse collects your blood sample at home, and final results take 3–4 weeks.
We dispatch a DHA‑registered phlebotomist with a cold‑chain kit. You can also submit pre‑extracted DNA or a dried blood spot on an FTA card. Results are securely delivered via our patient portal.
س: كيف تُجمع العينة وما هو وقت النتيجة؟
ج: تأتي ممرضة مرخصة إلى منزلك لسحب عينة دم، وتظهر النتائج النهائية خلال 3–4 أسابيع.
Q: What happens if my test result is positive?
A: A positive result leads to immediate clinical referral for lifelong monitoring and family cascade testing.
You will be connected to an on‑site DHA haematologist‑oncologist who will design a personalised surveillance plan, including periodic blood counts and imaging. First‑degree relatives can then undergo cascade testing under genetic counselling.
س: ماذا يحدث إذا كانت نتيجة الاختبار إيجابية؟
ج: تحويل فوري إلى أخصائي أمراض الدم للمراقبة مدى الحياة وإجراء الفحوصات للعائلة.
Regulatory Compliance: This service adheres to UAE Federal Decree‑Law No. 41 of 2024 (Art. 87), CDS Law 2026 (Minors’ genetic testing), and UAE PDPL (Federal Decree‑Law No. 45 of 2021). Your data is protected under DHA‑licensed Facility No. 9834453. Methodology: NGS with Sanger‑validated variant calling. All procedures comply with ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139).
Pre‑ requirement: A mandatory genetic counselling session to construct a three‑generation pedigree. No dietary or medication restrictions are required for blood collection.
دعم ثنائي اللغة متاح
التحقق من التغطية التأمينية
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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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