Test Price
2,800 AED✅ Home Collection Available
PROS1 Gene Protein S Deficiency Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين PROS1 لنقص بروتين S في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
الملخص التنفيذي
يقدم مركزنا اختبار تسلسل الجيل التالي لجين PROS1 المرتبط بنقص بروتين S الوراثي السائد، بدقة تشخيصية 99.9% وفق معايير هيئة الصحة بدبي لعام 2026، مع خدمة السحب المنزلي المعتمدة وتوجيه ما بعد الفحص.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing.
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection and VIP Mobile Phlebotomy.
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in Result Interpretation.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview
This advanced Next-Generation Sequencing (NGS) genetic test screens the entire PROS1 gene for pathogenic variants causing autosomal dominant Protein S deficiency, a major inherited risk factor for venous thromboembolism. In the UAE, this test provides definitive molecular diagnosis and guides personalized thromboprophylaxis.
| Parameter | Our Test (NGS Full Gene) | Closest Alternative (Functional Assay) |
|---|---|---|
| Precision | >99.9% analytical sensitivity & specificity for nucleotide variants | ~95% sensitivity; influenced by acute phase reactions, anticoagulants |
| Methodology | NGS (LC-MS/MS validated for complex regions) | Clotting-based (PTT-based) functional protein S activity |
| Turnaround Time | 3 to 4 Weeks | 3–5 working days |
Physician Insight & Safety Protocol
Note from Dr. PRABHAKAR REDDY (DHA: 61713011): Genetic testing for Protein S deficiency must be interpreted in the context of personal and family history of thrombosis. A positive result identifies an inherited predisposition, not a current clot, and requires careful clinical correlation. I emphasize that this test is a molecular diagnostic tool — always discuss results with your treating specialist before making any health decisions.
⚠️ Important: Do not discontinue prescribed anticoagulants or other medications without consulting your doctor. This genetic test does not replace acute clinical management.
Patient Safety: Exclusion Criteria & Emergency Red Flags
- This test is not intended for individuals currently experiencing an acute thrombotic event (deep vein thrombosis, pulmonary embolism) — seek immediate emergency care.
- Not suitable as a point-of-care test; does not provide real-time clotting status.
- Patients with a recent blood transfusion or bone marrow transplant may have donor DNA interference — consult lab before sample collection.
- Red Flag Symptoms: sudden chest pain, shortness of breath, leg swelling with redness/warmth, coughing up blood — call 998 or visit the nearest emergency room immediately.
UAE Regulatory & Quality Assurance
This service is fully compliant with Federal Decree-Law No. 41 of 2024 (Art. 87) on the protection of health data, the UAE Child Data Safety Law 2026 for minors, and the Personal Data Protection Law (PDPL). Our facility (License: 9834453) is ISO 9001:2015 certified (Cert: INT/EGQ/2509DA/3139), ensuring stringent quality management. All genetic data is encrypted and retained under strict confidentiality protocols.
Frequently Asked Questions
1. How does the PROS1 NGS test differ from a standard protein S functional assay? (ما الفرق بين اختبار جين PROS1 وفحص بروتين S الوظيفي؟)
This Genetic Test provides a stable, lifetime result unaffected by transient conditions. A positive genetic finding confirms the hereditary nature and guides family screening.
2. Can I take this test if I am currently on blood thinners? (هل يمكنني إجراء الاختبار أثناء تناول مميعات الدم؟)
Yes, because the PROS1 Genetic genetic counseling. The sample can be collected as whole blood, extracted DNA, or a dried blood spot, making it convenient even for patients on chronic therapy.
3. What is the turnaround time and how will I receive my results? (كم يستغرق ظهور النتائج وكيف أتسلمها؟)
Results are delivered within 3 to 4 weeks via a secure encrypted PDF report, accompanied by a complimentary telephonic interpretation session with a specialist. The report details detected variants, pathogenicity classification, and clinical correlation recommendations. We also offer a family pedigree mapping as part of the genetic counseling package, ensuring you and your loved ones understand the inheritance pattern and necessary preventive measures.
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Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians