Test Price
2,800 AED✅ Home Collection Available
BMPR1A Gene Hereditary Mixed Polyposis Syndrome Type 2 (HMPS2) Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين BMPR1A لمتلازمة السلائل الوراثية المختلطة من النوع الثاني (HMPS2) في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary & Clinical Confidence
- Accuracy Guarantee: 99.9% diagnostic sensitivity via ISO 9001:2015 accredited NGS processing.
- الفحص الجيني لجين BMPR1A بدقة تشخيصية 99.9% عبر مختبر معتمد آيزو 9001:2015.
- Premium Logistics: Paid hospital-grade home collection with ISO certified cold-chain transport and VIP mobile phlebotomy.
- Clinical Guidance: Complimentary telephonic post-test clinical interpretation of results with a genetic counsellor.
- Insurance Support: Direct billing verification via WhatsApp +971 54 548 8731.
Overview
This advanced NGS (Genetic Testinal polyps. تحليل جيني متطور للكشف المبكر عن المتلازمة الوراثية وتقييم خطر الإصابة بسرطان القولون.
| Feature | Our Test (NGS) | Closest Alternative (Single‑Site/Sanger) |
|---|---|---|
| Precision | Full gene sequencing; detects point mutations, indels, and copy number variants | Targeted mutation hot‑spots only; limited CNV detection |
| Methodology | Next Generation Sequencing (Illumina platform) | Sanger sequencing or PCR‑based single exon analysis |
| Turnaround Time | 3–4 Weeks (comprehensive analysis) | 2–4 weeks (limited targets) |
*All times exclude sample transit. Rush processing available on request.
Physician Insight & Safety Protocol
“A positive BMPR1A result opens the door for life‑saving colonoscopic surveillance; a negative result, however, does not erase the family legacy—clinical correlation with a detailed pedigree remains paramount. I urge you to view this test not as a standalone answer, but as a compass that guides personalised prevention. Your story matters, and we are honoured to walk this path with you.”
— Dr. PRABHAKAR REDDY, DHA License 61713011, Consultant Clinical Geneticist
⚠️ Do not discontinue any prescribed medication or alter your treatment plan without direct consultation with your treating physician.
Exclusion Criteria & Emergency Red Flags
- Exclusion: Active chemotherapy or recent blood transfusion (within 2 weeks) that may compromise DNA integrity; inability to provide informed consent; or incomplete pre‑test genetic counselling session.
- Emergency Red Flags: Sudden, severe abdominal pain; rectal bleeding or melena; signs of bowel obstruction (vomiting, distension). If any of these occur, seek immediate emergency medical attention—do not wait for test results.
Patient FAQ & Clinical Guidance
What is the BMPR1A gene test and why is it done?
Snippet Answer: The BMPR1A NGS test detects inherited mutations in the BMPR1A gene that cause hereditary mixed polyposis syndrome, significantly raising colorectal cancer risk.
It is indicated for individuals with a personal or family history of multiple and/or mixed gastrointestinal polyps, early‑onset colorectal cancer, or a known familial BMPR1A mutation. Early identification enables tailored endoscopic surveillance and risk‑reduction strategies. اختبار جين BMPR1A يكشف الطفرات الموروثة المسببة لمتلازمة السلائل الوراثية المختلطة لتوجيه المراقبة الوقائية.
Who should consider undergoing this genetic test?
Snippet Answer: Anyone with multiple mixed colon polyps, a strong family history of colorectal cancer, or a first‑degree relative with a known BMPR1A mutation should consider testing.
The test is also valuable for at‑risk relatives to clarify their own cancer predisposition and for families seeking peace of mind when a hereditary pattern is suspected. يُنصح بالفحص للأشخاص ذوي التاريخ العائلي القوي لسرطان القولون أو السلائل المتعددة لتحديد الخطر الوراثي.
How do I prepare for the test and what can I expect?
Snippet Answer: No fasting is required, but you must complete a pre‑ genetic counselling session to document your family history and sign informed consent.
A simple blood sample (or DNA from FTA card) is collected via our home phlebotomy service; results are ready in 3–4 weeks and a genetic counsellor will explain the findings in a follow‑up teleconsultation. جلسة استشارة وراثية قبل الفحص إلزامية، ثم يُسحب عينة دم بسيطة للحصول على النتائج خلال ٣-٤ أسابيع.
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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.
Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians