Test Price
2,800 AED✅ Home Collection Available
BMPR2 Gene – Pulmonary Hypertension, Primary Type (Genetic Test) in UAE | 2800 AED | 2026 DHA Guidelines
تحليل الجين BMPR2 لارتفاع ضغط الدم الرئوي الأولي في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary
This comprehensive NGS-based genetic test identifies pathogenic variants in the BMPR2 gene, enabling definitive diagnosis of heritable pulmonary arterial hypertension (HPAH). Performed under DHA License 9834453 with ISO 9001:2015 certification, the test delivers 99.9% diagnostic sensitivity, guiding life-saving clinical decisions and family risk assessment.
يقدم هذا الاختبار الجيني الشامل تشخيصاً دقيقاً لارتفاع ضغط الدم الرئوي الوراثي، معتمداً من هيئة الصحة بدبي وبمعايير الجودة العالمية.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO-Accredited NGS Processing.
- Premium Logistics: Hospital-Grade Home Collection (8 AM–11 PM) with ISO-Certified Cold-Chain Transport.
- Clinical Guidance: Telephonic Post-Test Interpretation by a Senior Clinical Geneticist.
- Insurance: Direct Billing Verification – WhatsApp +971 54 548 8731.
Overview – Why This Test Matters
The BMPR2 NGS test identifies DNA variants linked to primary pulmonary hypertension, a rare vascular disease with high mortality if undetected. It is the gold standard for confirming hereditary predisposition and informing targeted surveillance in at-risk family members.
يُعد اختبار الجين BMPR2 المعيار الذهبي لتأكيد الاستعداد الوراثي لارتفاع ضغط الدم الرئوي الأولي، مما يساعد في الكشف المبكر والمراقبة العائلية.
| Feature | Our Test (NGS) | Closest Alternative (Single-Gene Sanger) |
|---|---|---|
| Precision | Full gene coverage, deep intronic & regulatory regions | Coding exons only |
| Methodology | Next-Generation Sequencing + AI-validated bioinformatics | Capillary electrophoresis (Sanger) |
| Speed | 3–4 Weeks (faster with family linkage) | 6–8 Weeks |
| Clinical Utility | Actionable for early intervention & cascade testing | Limited; often requires further testing |
Physician Insight & Safety Protocol
“As a clinician, I appreciate the anxiety a pulmonary hypertension workup can bring. This genetic test provides powerful, actionable data, but it must be interpreted alongside echocardiographic and hemodynamic findings. I remain your partner in crafting a safe, personalized care path.”
— Dr. PRABHAKAR REDDY, DHA License 61713011
⚠ Medical Warning
Do not discontinue prescribed medication or alter your treatment plan without consulting your doctor. Genetic results guide, not replace, clinical judgement.
Safety Exclusion Criteria & Red Flags
- Exclusion: Testing of asymptomatic minors without prior genetic counselling; use for insurance eligibility decisions; self‑collection without valid DHA referral.
- Emergency Red Flags: New‑onset severe dyspnea at rest, syncope, chest pain, or signs of right heart failure – seek immediate emergency care, do not wait for genetic results.
- Mandatory Pre‑Test: A formal genetic counselling session and a three‑generation pedigree must be completed before sample collection.
Patient FAQ & Clinical Guidance
Q1: What is the BMPR2 gene test, and why is it done?
The BMPR2 gene test detects DNA changes causing heritable pulmonary arterial hypertension, enabling early diagnosis and family screening. It is recommended when you have unexplained pulmonary hypertension or a family history of the disease. The test uses a blood sample or extracted DNA and helps your doctor determine the best surveillance or treatment strategy.
س1: ما هو اختبار الجين BMPR2 ولماذا يتم إجراؤه؟
يكشف اختبار الجين BMPR2 عن التغيرات الوراثية المسببة لارتفاع ضغط الدم الرئوي الوراثي، مما يسمح بالتشخيص المبكر وفحص أفراد الأسرة. يُوصى به عند وجود ارتفاع ضغط رئوي غير مفسر أو تاريخ عائلي للمرض، ويُجرى من عينة دم بسيطة.
Q2: How is the test performed, and how long do results take?
A hospital-grade phlebotomist collects a blood sample at your home, and results are ready in 3–4 weeks. You may also provide extracted DNA or a drop of blood on an FTA card. Once the sample reaches our ISO‑certified lab, Next‑Generation Sequencing is performed, followed by expert analysis. You will receive a secure report interpreted by a clinical geneticist, with direct physician follow‑up.
س2: كيف يتم إجراء الاختبار وكم يستغرق ظهور النتائج؟
يقوم أخصائي سحب دم مرخص بزيارتك منزلياً، وتظهر النتائج خلال 3–4 أسابيع. يمكنك أيضاً تقديم عينة حمض نووي مستخلص أو بقعة دم على بطاقة FTA، وبعد الفحص المخبري بتقنية التسلسل الجيني المتقدم يصلك تقرير معتمد.
Q3: What do the results mean for my family?
A positive result indicates a heritable risk that can be tested in relatives, enabling lifesaving preventive monitoring. We strongly recommend cascade genetic testing for first‑degree family members. Even if you negative, clinical surveillance may continue if you have symptoms or other risk factors. All family discussions should occur under the guidance of a certified genetic counsellor.
س3: ماذا تعني النتائج لعائلتي؟
تشير النتيجة الإيجابية إلى خطر وراثي يمكن فحصه لدى الأقارب، مما يتيح مراقبة وقائية منقذة للحياة. نوصي بشدة بإجراء اختبار متسلسل لأفراد الأسرة من الدرجة الأولى، ويجب أن تتم جميع الاستشارات تحت إشراف مستشار وراثي معتمد.
UAE Regulatory & Quality Compliance
This service strictly adheres to Federal Decree-Law No. 41 of 2024 (Art. 87), CDS Law 2026 (Minors protection), and UAE PDPL for data privacy. All testing is performed in an ISO 9001:2015 certified facility (Cert: INT/EGQ/2509DA/3139) under DHA clinical governance.
ISO 9001:2015
Cert: INT/EGQ/2509DA/3139
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.
Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians