Test Price
2,800 AED✅ Home Collection Available
PALB2 Gene Fanconi Anemia Type N Genetic Test (NGS) in UAE | 2800 AED | 2026 DHA Guidelines
تحليل طفرة جين PALB2 المرتبطة بفقر دم فانكوني النوع N باستخدام تقنية التسلسل الجيني من الجيل التالي (NGS) في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary – Your High‑Precision Genetic Reality Check
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO‑Accredited Next‑Generation Sequencing (NGS) – powered by Illumina NovaSeq™ chemistry and validated against ClinVar 2026 reference datasets.
- Premium Logistics: Paid Hospital‑Grade Home Collection via ISO‑Certified Cold‑Chain Home Collection & VIP Mobile Phlebotomy (available 8 AM – 11 PM daily).
- Clinical Guidance: Complimentary Telephonic Post‑Test Clinical Guidance with a DHA‑licensed genetic counsellor to interpret your report securely.
- Insurance Support: Direct Billing Verification – WhatsApp your Emirates ID & policy card to +971 54 548 8731 for instant confirmation.
الملخص التنفيذي: يوفر هذا التحليل تشخيصاً دقيقاً لطفرة جين PALB2 المرتبطة بفقر دم فانكوني من النوع N، مع تقييم قابلية الإصابة بالأورام الوراثية. الإجراء معتمد من هيئة الصحة بدبي وحاصل على شهادة ISO 9001:2015، ويتضمن خدمة جمع العينات من المنزل واستشارة طبية متخصصة بعد ظهور النتائج.
Test Overview
The PALB2 Gene Fanconi Anemia Type N Genetic Test uncovers pathogenic germline variants in the PALB2 tumour‑suppressor gene using NGS, enabling early diagnosis of Fanconi anaemia type N and precise assessment of hereditary breast and pancreatic cancer risks. يكشف التحليل الطفرات الجينية في جين PALB2 المرتبط بفقر دم فانكوني النوع N ويساعد في تقييم مخاطر السرطان الوراثي.
| Parameter | Our Test – ISO‑Accredited NGS | Closest Alternative – Single‑Gene Sanger Sequencing |
|---|---|---|
| Precision | Full coding region ± 20 bp intronic boundaries – >99% analytical sensitivity | Targeted exon‑only analysis; may miss deep intronic or large deletions |
| Methodology | Illumina Next‑Generation Sequencing (NGS) with proprietary bioinformatics pipeline | Sanger sequencing – lower throughput, limited variant resolution |
| Turnaround Time | 3–4 Weeks from sample receipt | 4–6 Weeks |
Physician Insight & Safety Protocol
“As a DHA‑licensed hematologist (Dr. Prabhakar Reddy, DHA: 61713011), I emphasise that a PALB2 genetic result is a clinical compass, not a verdict. Always correlate this finding with a complete history, physical examination, and family pedigree; a negative report does not abolish the need for cancer surveillance in high‑risk families. If you are already on chemodeterrent or hormonal therapy, never self‑discontinue – discuss any report interpretation only with your treating specialist.”
⚠️ Medication Warning: Do not discontinue prescribed medication without consulting your doctor.
🛑 Safety Information & Exclusion Criteria
- This test is not suitable for fetal screening without prior genetic counselling and invasive sampling protocols.
- Patients who have received a blood transfusion within 14 days may require DNA isolation from an alternative sample (buccal swab) to avoid donor DNA interference.
- Minors (≤18 years) require consent from both legal guardians in accordance with UAE CDS Law 2026 – please contact our team before booking.
- Urgent red flags: If you experience unexplained bruising, severe fatigue, recurrent infections, or signs of bone marrow failure before your appointment, seek emergency medical attention immediately – do not wait for genetic results.
Patient FAQ & Clinical Guidance
What is the PALB2 Gene Fanconi Anemia Type N Genetic Test used for?
This test identifies pathogenic germline variants in the PALB2 gene that cause Fanconi anemia type N and significantly increase breast and pancreatic cancer risk. The analysis guides precision oncology surveillance and family planning. يكشف هذا الفحص الطفرات الجينية المسببة لفقر دم فانكوني النوع N ويساعد في تقدير خطر الأورام السرطانية للإرشاد الوراثي وتخطيط الأسرة.
How long does it take to receive the results?
The standard turnaround time is 3 to 4 weeks from the arrival of your sample at our ISO‑certified laboratory. Complex variants needing orthogonal confirmation may add up to 7 days; you will be notified proactively. تتراوح مدة ظهور النتائج بين 3 و4 أسابيع من وصول العينة إلى المختبر المعتمد، مع إشعار فوري في حال الحاجة لتأكيدات إضافية.
Is genetic counselling included before or after the test?
Yes, a pre‑test genetic counselling session is mandatory to draw a detailed multigenerational pedigree and ensure informed consent. Post‑ telephonic guidance with a DHA‑licensed counsellor is included to clarify results and next steps. نعم، الجلسة الإرشادية قبل الفحص إلزامية لرسم شجرة العائلة وتوثيق الموافقة المستنيرة، تليها استشارة هاتفية بعد النتائج.
UAE Compliance & Accreditation
- Licensed Medical Facility (MOHAP Code 9834453) – regulated under Federal Decree‑Law No. 41 of 2024 (Medical Liability) and UAE PDPL (Federal Decree‑Law No. 45 of 2021).
- All testing adheres to ISO 9001:2015 Quality Management System (Cert: INT/EGQ/2509DA/3139).
- Home collection service operates under Community Development Sector (CDS) Law 2026 provisions for minors.
- Data privacy: personal health information never shared without explicit consent; encrypted pipeline per UAE Information Assurance standards.
دعم ثنائي اللغة متاح
التحقق من التغطية التأمينية
Check Insurance Coverage Instantly
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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ISMS 27001:2022
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All reports reviewed by DHA-Certified physicians