Test Price
2,800 AED✅ Home Collection Available
TGM6 Gene Sequencing Test for Spinocerebellar Ataxia Type 35 (SCA35), Autosomal Dominant in UAE | AED 2800 | 2026 DHA Guidelines
تحليل جين TGM6 للرنح المخيخي الشوكي النوع 35 (SCA35) السائد جسمياً في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO-certified NGS 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.
ضمان دقة تشخيصية بنسبة 99.9% عبر مختبرات معتمدة وفق معايير الآيزو، مع خدمة سحب منزلي متميزة وإرشاد طبي بعد الفحص.
Overview
This advanced next-generation sequencing (NGS) test analyzes the entire coding region of the TGM6 gene to detect pathogenic variants responsible for spinocerebellar ataxia type 35 (SCA35), an autosomal dominant neurodegenerative disorder. يكشف هذا الاختبار الجيني المتطور عن الطفرات المسببة للرنح المخيخي الشوكي النوع 35 بدقة عالية.
| Feature | Our Test (TGM6 NGS) | Closest Alternative (Multi-Gene Ataxia Panel) |
|---|---|---|
| Precision | Single-gene deep sequencing with >99% analytical sensitivity | Broad coverage but may miss deep intronic variants in TGM6 |
| Methodology | NGS (Illumina platform) with full Sanger confirmation of pathogenic findings | Whole Exome Sequencing/panel-based NGS |
| Turnaround Time | 3–4 Weeks | 4–6 Weeks (often requires reflex to single-gene testing) |
Physician Insight & Safety Protocol
"As a clinical neurologist, I understand that considering genetic testing for SCA35 can be emotionally challenging. This NGS test provides definitive molecular confirmation, enabling precise prognosis and family planning. Always correlate findings with clinical evaluation for comprehensive care."
— Dr. PRABHAKAR REDDY, DHA License No. 61713011
Medication Warning:
Do not discontinue prescribed medication without consulting your doctor. Genetic test results are intended to complement clinical management, not replace it.
Safety & Exclusion Criteria
- Exclusion Criteria: Individuals with acute encephalopathy or uncontrolled seizures that may interfere with informed consent. Patients unable to undergo venipuncture or provide DNA sample.
- ER Red Flags (seek immediate emergency care; this genetic test is not for acute diagnosis): Rapidly worsening ataxia with loss of independent ambulation within weeks, new‑onset dysphagia with aspiration risk, acute vision loss, severe headache, or altered consciousness.
Patient FAQ & Clinical Guidance
What is the TGM6 gene test for SCA35?
The TGM6 sequencing test detects pathogenic variants in the TGM6 gene causing spinocerebellar ataxia type 35, an autosomal dominant disorder.
يكشف اختبار تسلسل جين TGM6 عن الطفرات المسببة للرنح المخيخي الشوكي النوع 35 الوراثي السائد.
How should I prepare for the test?
Provide a detailed clinical history of ataxia symptoms and neurological examination findings; genetic counselling with a pedigree chart is required before sample collection.
يجب تقديم تاريخ سريري مفصل لأعراض الرنح وجلسة استشارة وراثية لرسم شجرة العائلة قبل جمع العينة.
Can the be used for prenatal or predictive testing?
Yes, after thorough genetic counselling and informed consent, it can be applied in predictive or prenatal settings following UAE genetic testing regulations.
نعم، بعد استشارة وراثية شاملة وموافقة مستنيرة، يمكن استخدامه في الفحوصات التنبؤية أو ما قبل الولادة وفقاً لقوانين الفحص الجيني الإماراتية.
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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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