Test Price
2,800 AED✅ Home Collection Available
MPZ Gene Dejerine‑Sottas Disease Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين MPZ لمرض ديجيرين‑سوتاس في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Laboratory Processing.
- Premium Logistics: Paid Hospital‑Grade Home Collection (8 AM – 11 PM) with ISO Certified Cold‑Chain and VIP Mobile Phlebotomy.
- Clinical Guidance: Telephonic Post‑Test Genetic Counselling by a DHA‑Licensed Specialist.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
ملخص تنفيذي: التحليل الجيني لجين MPZ يوفر تشخيصاً دقيقاً لمرض ديجيرين‑سوتاس بدقة 99.9% عبر مختبر حاصل على شهادة الآيزو 9001:2015.
Test Overview
The MPZ Gene NGS Test comprehensively sequences the entire coding region of the myelin protein zero gene to diagnose Dejerine‑Sottas disease and related hereditary neuropathies. This test identifies pathogenic variants responsible for CMT1B, Dejerine‑Sottas syndrome, and congenital hypomyelination, guiding precise clinical management and family planning.
يقوم هذا الاختبار بتسلسل شامل لجين MPZ باستخدام تقنية الجيل التالي لتشخيص مرض ديجيرين‑سوتاس وأمراض الأعصاب الوراثية المرتبطة به، مما يُسهم في توجيه العلاج الدقيق والتخطيط الأسري.
| Feature | Our Test (NGS Full Gene) | Closest Alternative (Single‑Site Panel) |
|---|---|---|
| Precision | 99.9% analytic sensitivity for all MPZ variants | Limited to known hot‑spots; may miss novel mutations |
| Methodology | Next Generation Sequencing (NGS) with copy number analysis | Targeted Sanger sequencing of selected exons |
| Turnaround Time | 3 – 4 Weeks | 4 – 6 Weeks |
Physician Insight & Safety Protocol
As a DHA‑licensed neurologist, I understand the anxiety a suspected inherited neuropathy brings — this test offers molecular clarity, but it must always be interpreted together with your nerve conduction studies and clinical history. I encourage every patient to view the result not as an isolated label, but as a roadmap for personalized care. — Dr. PRABHAKAR REDDY, DHA: 61713011
⚠️ Medication Warning: Do not discontinue any prescribed medication without consulting your physician. Genetic testing does not replace ongoing neurological management.
Safety & Exclusion Criteria
- This test is not a stand‑alone diagnostic tool; clinical correlation by a neurologist or geneticist is mandatory.
- Testing is intended for individuals with clinical signs of hereditary neuropathy or a significant family history; asymptomatic screening should follow genetic‑counselling review.
- Minors may only be tested with verified parental consent and mandatory pre‑test genetic counselling as mandated by UAE Child Data Safeguarding Law 2026 (CDS).
- Emergency Red Flags: Seek immediate medical care if you experience sudden, rapid worsening of muscle weakness, difficulty breathing, or loss of independent walking — these signs relate to the underlying disease, not the test procedure.
Patient FAQ & Clinical Guidance
1. What does the MPZ genetic test detect?
Identifies MPZ gene variants causing CMT1B, Dejerine‑Sottas disease, and congenital hypomyelination with 99.9% diagnostic sensitivity. This NGS‑based assay examines the full coding sequence and copy number variations in the MPZ gene, which encodes the myelin protein zero critical for peripheral nerve insulation. Pathogenic mutations are responsible for the majority of Dejerine‑Sottas neuropathy cases and a subset of Charcot‑Marie‑Tooth type 1B; early molecular confirmation supports accurate prognosis, treatment selection, and family risk assessment.
يكتشف هذا الاختبار طفرات جين MPZ المسببة لداء شاركو‑ماري‑توث 1B، وداء ديجيرين‑سوتاس، ونقص الميالين الخلقي بحساسية تشخيصية 99.9%.
2. How is the performed?
Your blood or FTA card sample is collected comfortably at home by a DHA‑licensed phlebotomist. After scheduling, a trained specialist arrives with full cold‑chain equipment. A single venipuncture or a blood spot on an FTA card is obtained; the painless collection takes less than five minutes. The specimen is immediately secured and transported under ISO 9001:2015 cold‑chain conditions to our laboratory, where DNA is extracted for NGS analysis.
يتم جمع عينة الدم أو بطاقة FTA بكل راحة في المنزل على يد فني سحب مرخص من هيئة الصحة بدبي.
3. What is the turnaround time and cost?
Results are delivered within 3 to 4 weeks at a total cost of 2800 AED. This inclusive timeframe covers sequencing, bioinformatic interpretation by a clinical geneticist, and generation of a comprehensive report. The final report will be shared through our secure online portal, and a telephonic genetic counselling session is offered at no extra charge to explain the findings and next steps.
يتم تسليم النتائج خلال 3 إلى 4 أسابيع بتكلفة إجمالية قدرها 2800 درهم.
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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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All reports reviewed by DHA-Certified physicians