Test Price
2,800 AED✅ Home Collection Available
MTOR Gene Sequencing for Neurodevelopmental Disorders in UAE | 2,800 AED | 2026 DHA Guidelines
تحليل طفرة جين MTOR للاضطرابات النمائية العصبية في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
الملخص التنفيذي: يوفر فحص تسلسل الجينوم المتقدم لتحديد طفرات جين MTOR المرتبطة بالاضطرابات النمائية العصبية حساسية تشخيصية تبلغ 99.9% عبر مختبر معتمد آيزو 9001:2015. خدمة سحب الدم المنزلي بتقنية التبريد المتقدم. استشارة طبية بعد الفحص. التحقق من التأمين عبر واتساب: +971545488731.
- ✔ Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Certified Cold‑Chain Processing.
- ✔ Premium Logistics: Hospital‑Grade Home Collection & VIP Mobile Phlebotomy (8 AM – 11 PM).
- ✔ Clinical Guidance: Telephonic Post‑Test Clinical Guidance with DHA‑Licensed Genetic Counsellor.
- ✔ Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Clinical Overview
The MTOR gene sequencing test analyzes the entire coding region of the MTOR gene using Next‑Generation Sequencing (NGS) to detect pathogenic variants associated with neurodevelopmental disorders, including macrocephaly, intellectual disability, and epilepsy. (تحليل تسلسل جين MTOR يكشف الطفرات المسببة للاضطرابات العصبية النمائية). This definitive molecular diagnosis empowers clinicians to tailor surveillance, therapy, and familial recurrence risk counselling in full compliance with DHA standards.
| Feature | Our Test – NGS Pro | Closest Alternative (Sanger‑only) |
|---|---|---|
| Methodology | Next‑Generation Sequencing (NGS) + Sanger confirmation | Sanger sequencing (limited hotspot regions) |
| Gene Coverage | All exons & splice sites of MTOR | Selected exons only |
| Turnaround Time | 3‑4 weeks | 6‑8 weeks |
| Sample & Logistics | Blood, DNA, or FTA card – Home collection available | Blood only – In‑clinic draw |
Physician Insight & Safety Protocol
“This genetic test offers a critical window into the molecular basis of your or your child’s neurodevelopmental condition. Clinical correlation with detailed phenotypic assessment and genetic counseling is paramount before interpreting results. A multidisciplinary team will guide you through the implications.”
— Dr. PRABHAKAR REDDY, DHA License: 61713011, Consultant Neurologist & Clinical Geneticist
‼ Medication Safety Advisory
Do not discontinue any prescribed medication without consulting your treating physician. Genetic test results must be integrated into the overall clinical picture and never used alone to alter treatment.
Patient Exclusion Criteria & Emergency Red Flags
- Exclusion Criteria: Active chemotherapy or blood transfusion within 2 weeks may affect DNA quality; alternative sample type (buccal swab) may be advised. This test is not indicated for asymptomatic individuals without a clinical indication of a neurodevelopmental disorder.
- Emergency Red Flags: If the patient experiences sudden neurological deterioration (uncontrolled seizures, loss of consciousness, acute weakness), seek immediate emergency care – this test is a scheduled diagnostic procedure, not an emergency intervention.
Patient FAQ & Clinical Guidance
1. What does the MTOR gene test detect? / ماذا يكشف فحص جين MTOR؟
This advanced genomic test identifies disease‑causing mutations in the MTOR gene linked to neurodevelopmental conditions, enabling precise clinical diagnosis and personalized treatment planning.
يكشف فحص جين MTOR عن الطفرات الممرضة (الجينية) المسؤولة عن اضطرابات النمو العصبي مثل كبر حجم الرأس والإعاقة الذهنية والصرع.
2. How is the sample collected and what is the turnaround time? / كيف يتم جمع العينة وما هي مدة النتائج؟
A simple blood draw or finger‑prick FTA card collection is performed at home by a licensed phlebotomist, with results ready in 3–4 weeks.
يتم أخذ عينة دم بسيطة أو وخز إصبع على بطاقة FTA في المنزل بواسطة فني معتمد، وتظهر النتائج خلال ٣ إلى ٤ أسابيع.
3. Is this test covered by UAE health insurance? / هل يغطي التأمين الصحي هذا الفحص؟
Most UAE insurance policies cover genetic testing for medically indicated neurodevelopmental disorders; direct billing verification is available via WhatsApp.
معظم وثائق التأمين في الإمارات تغطي الفحوصات الجينية للحالات النمائية العصبية المثبتة طبياً؛ يمكن التحقق من التغطية عبر واتساب.
Pre‑ requirement: A genetic counselling session and a pedigree chart of family members affected by MTOR‑related neurodevelopmental disorders are mandatory before sample collection.
دعم ثنائي اللغة متاح
التحقق من التغطية التأمينية
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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.
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