Test Price
1,500 AED✅ Home Collection Available
Spinocerebellar Ataxia (SCA) Genetic Profile (4 Markers) Test in UAE | 1500 AED | 2026 DHA Guidelines
تحليل ملف جينات الترنح النخاعي المخيخي (SCA) رباعي الواسمات في الإمارات | 1500 درهم | معتمد من هيئة الصحة بدبي
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.
ضمان دقة بنسبة 99.9% عبر مختبر معتمد وفق الأيزو، وخدمة سحب منزلي راقية، واستشارة هاتفية بعد الاختبار.
Overview
Spinocerebellar Ataxia (SCA) Profile (4 Markers) Test is a genetic test that screens for four common SCA-associated gene expansions using PCR and fragment analysis, aiding in definitive diagnosis of hereditary ataxia and guiding genetic counselling. يُستخدم تحليل ملف الطفرات الوراثية للترنح النخاعي المخيخي لتشخيص المرض وتوجيه الاستشارة الوراثية.
| Feature | Our Test (4 Markers) | Alternative (Single Gene) |
|---|---|---|
| Precision (Analytical Sensitivity) | 99.9% (PCR Fragment Analysis) | ~95% (Sanger sequencing of one locus) |
| Methodology | PCR + Fragment Analysis (GeneScan/STR) | PCR + Sanger Sequencing |
| Turnaround Time | Report by Saturday (sample Tue by 11 am) | 7–10 days |
| Covered Markers | SCA1, SCA2, SCA3, SCA6 (or any 4) | One gene at a time |
Physician Insight & Safety Protocol
“This test provides critical molecular confirmation of hereditary ataxia, but results must be interpreted alongside clinical examination and family history. A negative panel does not exclude all forms of ataxia, and broader panels may be warranted. I advise patients to follow up with a neurologist for comprehensive care.” — Dr. Prabhakar Reddy, DHA License 61713011.
Medication Warning: Do not discontinue prescribed medication without consulting your doctor.
Exclusion Criteria & ER Red Flags:
- Severe acute illness or hemodynamic instability – postpone collection.
- Recent blood transfusion (within 2 weeks) may interfere with germline DNA analysis.
- If experiencing sudden worsening of gait, vision, speech, or consciousness – seek emergency care immediately.
Pre‑Test Requirement: A duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory for sample acceptance.
Patient FAQ & Clinical Guidance
What is the purpose of the SCA 4‑marker genetic test?
This test detects pathogenic repeat expansions in the SCA1, SCA2, SCA3, and SCA6 genes that cause progressive cerebellar ataxia, enabling definitive diagnosis and genetic counseling. يكشف هذا التحليل عن التوسعات المتكررة المسببة للمرض في أربعة جينات رئيسية، مما يؤكد التشخيص ويوجه الاستشارة الوراثية.
How do I prepare for the blood draw?
No fasting is required; simply ensure the Duly filled Genomics Clinical Information Requisition Form (Form 20) is completed and present for collection. لا يلزم الصيام، ولكن يجب ملء استمارة المعلومات السريرية الجينومية (نموذج 20) قبل سحب العينة.
When will I receive my results, and how will they be delivered?
If the sample is received by Tuesday 11 am, the report is issued on Saturday; results are delivered via secure online portal and a telephonic post‑ guidance session with a clinical expert. تُصدر النتائج يوم السبت إذا وصلت العينة قبل الثلاثاء الساعة 11 صباحًا، وتُرسل عبر بوابة آمنة مع جلسة استشارية هاتفية.
ISO 9001:2015 Certified (Cert: INT/EGQ/2509DA/3139) | DHA Facility License: 9834453
Home Collection: 8 AM – 11 PM daily | WhatsApp: +971545488731
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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