Test Price
2,800 AED✅ Home Collection Available
CCT5 Gene Neuropathy (Hereditary Sensory with Spastic Paraplegia) Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل الجين CCT5 للاعتلال العصبي الحسي الوراثي مع الشلل السفلي التشنجي في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary of Your UAE Diagnostic Journey
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain transport. VIP Mobile Phlebotomy available 8 AM – 11 PM.
- Clinical Guidance: Telephonic Post-Test Clinical Guidance with result interpretation included.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Clinical Positioning
This Next-Generation Sequencing (NGS) test comprehensively analyzes the full coding region of the CCT5 gene to identify pathogenic variants linked to hereditary sensory neuropathy with spastic paraplegia, a progressive neurogenetic disorder. التحليل الجيني الكامل للجين CCT5 يكشف الطفرات المسببة للاعتلال العصبي الحسي الوراثي والشلل التشنجي.
| Feature | Our Test (DHA‑Accredited NGS) | Closest Alternative (Sanger Sequencing of Single Exons) |
|---|---|---|
| Precision | >99% coverage of entire CCT5 coding region; variant‑level resolution | Targeted regions only; may miss deep intronic or copy‑number changes |
| Method | NGS (Next‑Generation Sequencing) on Illumina platform, clinically validated | Sanger Sequencing, limited to pre‑defined exons |
| Turnaround | 3 to 4 weeks (comprehensive analysis & clinical report) | 4–6 weeks for multiple exons; non‑comprehensive |
Physician Insight & Safety Protocol
“As a neurologist, I understand the anxiety that comes with hereditary neuropathies. This test provides the molecular clarity needed to guide treatment, assess family risk, and plan for the future. I always emphasize that results must be correlated with your full clinical picture and genetic counselling.” – Dr. PRABHAKAR REDDY (DHA License: 61713011)
❗ Do not discontinue prescribed medication without consulting your doctor.
Patient Safety Exclusion Criteria & Emergency Red Flags
- Exclusion: If you have an active infection or are unable to provide a blood sample, contact our team to reschedule.
- Exclusion: This test is not for asymptomatic minors without explicit consent under UAE Child Rights Law (Wadeema’s Law) and CDS 2026 regulations; a pediatric clinical geneticist must be involved.
- ER Red Flag: If you experience sudden worsening of spasticity, loss of bladder control, or acute sensory loss, seek emergency care immediately.
Patient FAQ & Clinical Guidance
What is the CCT5 gene neuropathy NGS test?
This NGS test analyzes the entire CCT5 gene to detect mutations causing hereditary sensory neuropathy with spastic paraplegia.
يقوم هذا الفحص بتسلسل كامل لجين CCT5 لاكتشاف الطفرات المسببة للاعتلال العصبي الحسي الوراثي مع الشلل التشنجي.
Who should consider undergoing this genetic test?
Patients with unexplained sensory neuropathy and spastic paraplegia, especially those with a family history, should consider this.
يُنصح بالفحص للمرضى الذين يعانون من اعتلال عصبي حسي وشلل تشنجي غير مفسر، خاصة مع وجود تاريخ عائلي.
What are the sample requirements and turnaround time?
A single blood sample (whole blood, DNA, or FTA card) is collected; results are ready within 3 to 4 weeks.
يتم جمع عينة دم واحدة (دم كامل أو حمض نووي أو بطاقة FTA) وتصدر النتائج خلال 3 إلى 4 أسابيع.
Confidentiality: UAE PDPL (Federal Decree-Law No. 45 of 2021) & Human Genome Law No. 41 of 2024 (Art. 87). ISO 9001:2015 Certified. Facility License: 9834453. For support: +971545488731.
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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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All reports reviewed by DHA-Certified physicians