Test Price
2,800 AED✅ Home Collection Available
CDH15 Gene Mental Retardation, Autosomal Dominant Type 3 (MRD3) Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين CDH15 للتأخر العقلي (النوع السائد جسميًا 3) في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
الملخص التنفيذي: تحليل تسلسل الجيل التالي لجين CDH15 لتشخيص التأخر العقلي الجسمي السائد من النوع الثالث بدقة 99.9%، مع خدمة سحب الدم المنزلي ونتائج موثوقة وفق معايير ISO.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 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) test analyzes the CDH15 gene for pathogenic variants associated with autosomal dominant intellectual disability type 3 (MRD3), delivering a precise molecular diagnosis for patients with neurodevelopmental delay. يوفر هذا الاختبار الجيني الشامل تشخيصًا دقيقًا للاضطرابات العصبية الوراثية ويتيح التخطيط المبكر للعلاج.
| Feature | Our CDH15 NGS Test | Closest Alternative (Single‑Gene Sanger) |
|---|---|---|
| Precision | 99.9% variant detection with Sanger validation | ~95% for targeted region |
| Method | NGS + confirmatory Sanger sequencing | Sanger sequencing only |
| Turnaround Time | 3 – 4 weeks | 6 – 8 weeks |
Physician Insight & Safety Protocol
“As a clinical neurologist, I understand the deep concerns of families facing unexplained developmental delays. This test offers a definitive genetic answer, but it must be interpreted alongside clinical findings and family history, and a positive result should lead to comprehensive genetic counseling. Always consult your specialist before altering any therapy.”
— Dr. Prabhakar Reddy, DHA License No. 61713011
⚠️ Medication Warning
Do not discontinue prescribed medication without consulting your doctor. Genetic test results do not replace clinical management.
🩺 Safety Exclusion Criteria & Red Flags
- Severe coagulopathy or active bleeding disorder (contraindicates venipuncture).
- Uncontrollable seizures or acute neuroregression requiring emergency care.
- ER Red Flags: Sudden loss of consciousness, new‑onset weakness, status epilepticus — seek immediate medical attention before testing.
- Inability to provide a viable blood or DNA sample (alternative collection may be arranged).
Patient FAQ & Clinical Guidance
Q: What does the CDH15 gene test detect?
“The CDH15 NGS test identifies genetic mutations responsible for autosomal dominant intellectual disability type 3.” This test screens the entire coding region of the CDH15 gene using Next‑Generation Sequencing, providing a yes/no answer for pathogenic alterations linked to MRD3. A positive result helps clinicians tailor educational, therapeutic, and surveillance plans.
Q: How is the performed and when will I receive results?
“A blood sample or DNA on an FTA card is collected via a home phlebotomist, with results in 3-4 weeks.” After booking, a licensed mobile phlebotomist arrives at your location between 8 AM and 11 PM. The sample travels in a temperature‑controlled cold chain, and the ISO‑certified lab completes the analysis and clinical report within four weeks.
س: ما الذي يكشفه اختبار جين CDH15 بالتفصيل؟
“يكتشف اختبار تسلسل الجيل التالي لجين CDH15 الطفرات المسببة للإعاقة الذهنية الجسمية السائدة من النوع الثالث.” يُستخدم هذا التحليل لتأكيد التشخيص الجزيئي لدى المرضى الذين يعانون من تأخر في النمو العصبي، مما يسمح بوضع خطة علاجية وعائلية دقيقة وفق أحدث التوصيات.
Legal & Regulatory: Fully compliant with Federal Decree‑Law No. 41 of 2024 (Art. 87), UAE Child Protection Law (Minors consent), and UAE PDPL for data privacy. Laboratory ISO 9001:2015 Certification INT/EGQ/2509DA/3139.
DHA License No. 9834453. Contact via WhatsApp: +971 54 548 8731. Service hours 08:00 – 23:00.
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