Test Price
2,800 AED✅ Home Collection Available
MPZ Gene DI‑CMTD Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين MPZ (DI‑CMTD) عبر التسلسل الجيني المتقدم NGS في الإمارات | ٢٨٠٠ درهم | معتمد من هيئة الصحة بدبي
يُتيح تحليل جين MPZ المرتبط بمرض شاركو-ماري-توث (DI‑CMTD) تشخيصًا جينيًا دقيقًا بنسبة حساسية 99.9% عبر معالجتنا المعتمدة آيزو، مع خدمة سحب العينات المنزلي في جميع أنحاء الإمارات.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 accredited lab (Cert: INT/EGQ/2509DA/3139).
- Premium Logistics: Paid Hospital‑Grade Home Collection via ISO Certified Cold‑Chain, VIP Mobile Phlebotomy 8 AM‑11 PM across the UAE.
- Clinical Guidance: Telephonic Post‑Test Result Interpretation & Genetic Counselling included at no extra charge.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview
The MPZ gene (Myelin Protein Zero) mutation analysis for DI‑CMTD (Dominant Intermediate Charcot‑Marie‑Tooth Disease) employs Genetic Test delivers 99.9% diagnostic sensitivity and is the gold standard for genetic subtyping of MPZ‑related neuropathies. يكتشف هذا التحليل طفرات جين MPZ المسببة لاعتلال الأعصاب الوراثي بدقة عالية وبأعلى معايير التسلسل الجيني.
| Feature | Our MPZ NGS Test | Nearest Alternative (Whole Exome) |
|---|---|---|
| Targeted Gene | Full MPZ gene sequencing & copy number analysis | MPZ captured within broad exome (no focused depth) |
| Sensitivity | 99.9% for exon/intron variants | ~95% due to coverage gaps |
| Turnaround | 3‑4 weeks (express available) | 8‑12 weeks |
| Pre‑ & Post‑Test Support | Genetic counselling + pedigree charting included | Often minimal or separate fee |
| Price | 2800 AED | 3500‑5000 AED |
Physician Insight & Safety Protocol
“As a Clinical Pathologist with DHA license 61713011, I emphasize that while this genetic test identifies MPZ mutations with high precision, a negative result does not exclude other genetic or acquired neuropathies. All findings must be correlated with clinical examination, nerve conduction studies, and family history. Genetic counselling before and after testing is strongly advised to interpret the implications for you and your at‑risk relatives.” — Dr. PRABHAKAR REDDY
⚠️ Medication Warning: Do not discontinue any prescribed medication without consulting your neurologist. This test is diagnostic, not therapeutic.
Exclusion Criteria & Emergency Red Flags:
- Minors under 18 years without legal guardian consent (Federal Decree‑Law No. 3 of 2026, Child Data Protection).
- Pregnancy is not a contraindication, but genetic counselling must involve an obstetric specialist.
- If you experience sudden muscle weakness, respiratory difficulty, or vision loss, seek emergency care immediately — these may not be related to test delay.
- Samples will not be accepted if collected from non‑standard sites or without proper patient identification.
Patient FAQ & Clinical Guidance
1. What does the MPZ Gene DI‑CMTD NGS test diagnose?
MPZ NGS testing detects mutations responsible for dominant intermediate Charcot‑Marie‑Tooth disease and related neuropathies precisely. The comprehensive analysis identifies deep intronic and copy number variants that may be missed by standard panels, enabling definitive diagnosis and tailored management plans. يكشف هذا الاختبار عن الطفرات المسؤولة عن مرض شاركو-ماري-توث المتوسط السائد والاعتلالات العصبية ذات الصلة بدقة متناهية.
2. How do I prepare for the sample collection?
Mandatory genetic counselling with pedigree charting is required before blood draw; no fasting for test. Our certified phlebotomist will collect a small blood sample or accept pre‑extracted DNA at your home, with full ISO‑certified cold‑chain handling. يلزم إجراء استشارة وراثية إلزامية مع رسم شجرة العائلة قبل سحب العينة؛ ولا يحتاج الاختبار إلى صيام.
3. How long until I receive results, and what support is included?
Results are dispatched in three to four weeks, with post‑ teleconsultation by a neurologist included. The package covers a detailed genetic report, interpretive guidance, and recommendations for family screening under DHA‑regulated protocols. تُصدر النتائج خلال ثلاثة إلى أربعة أسابيع، وتشمل الباقة استشارة هاتفية مع طبيب أعصاب لتفسير التقرير وتوجيه الفحص العائلي.
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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