Test Price
2,000 AED✅ Home Collection Available
Spinocerebellar Ataxia (SCA) Genetic Panel (Types 1, 2, 3, 6, 7, 10 & 12) in UAE | 2000 AED | 2026 DHA Guidelines
تحليل الفَحْص الجيني للرَّنَح النُّخَاعِي المُخَيخي (SCA) الأنواع 1، 2، 3، 6، 7، 10، 12 في الإمارات | 2000 درهم | معتمد من هيئة الصحة بدبي
Executive Summary
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing.
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection & VIP Mobile Phlebotomy (8 AM – 11 PM).
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation by DHA-licensed neurologists.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
الملخص التنفيذي:
- ضمان الدقة: حساسية تشخيصية بنسبة 99.9% عبر معالجة معتمدة ISO 9001:2015.
- الخدمات اللوجستية المتميزة: سحب الدم المنزلي عالي الجودة عبر سلسلة تبريد معتمدة ISO وفريق تمريض متنقل VIP من 8 صباحاً إلى 11 مساءً.
- الإرشاد السريري: استشارة هاتفية بعد الاختبار لتفسير النتائج من قِبَل أطباء أعصاب مرخصين من هيئة الصحة بدبي.
- التأمين: التحقق المباشر من التأمين عبر واتساب +971545488731.
Overview
Spinocerebellar ataxia (SCA) genetic panel detects trinucleotide repeat expansions in 7 common SCA genes (1, 2, 3, 6, 7, 10, 12) to confirm clinical diagnosis, guide prognosis, and inform family planning. يوفر الفحص دقة عالية لتحديد الطفرات الجينية المسببة للرنح النخاعي المخيخي ويساعد في التخطيط الأسري والاستشارة الوراثية.
| Feature | Our Test | Closest Alternative (Standard Hospital) |
|---|---|---|
| Precision Methodology | Triplet Repeat Primed PCR (TP‑PCR) & Fragment Analysis by Capillary Electrophoresis | Conventional End‑Point PCR only |
| Turnaround Time | 5‑7 Days | 10‑14 Days |
| DHA‑Accredited Counselling | Included (Telephonic) | Often referral‑based only |
| Home Collection | ISO‑Certified Cold‑Chain, 8 AM‑11 PM | Limited hours, no guaranteed cold chain |
Physician Insight & Safety Protocol
“As a neurologist, I understand that genetic testing for ataxia can be emotionally challenging. This panel provides precise molecular diagnosis, but results must be interpreted in the context of your full clinical picture and family history. I always advise my patients to discuss findings with a trained genetic counsellor before making any life-altering decisions.”
— Dr. PRABHAKAR REDDY, DHA License 61713011 (Consultant Neurologist)
Patient Safety: Exclusion Criteria & Emergency Red Flags
- Exclusion Criteria: Pregnancy (except when medically indicated and ordered by an obstetrician/neurologist); individuals under 18 years without formal genetic counselling, informed parental consent, and DHA‑mandated minor‑specific legal compliance (CDS Law 2026); insufficient peripheral blood sample or visible hemolysis.
- ER Red Flags – Seek Immediate Emergency Care: Sudden onset of severe gait imbalance, difficulty swallowing (dysphagia), double vision (diplopia), slurred speech with respiratory difficulty, or altered consciousness.
Patient FAQ & Clinical Guidance
Q: What is the Spinocerebellar Ataxia Panel and why is it performed?
This test simultaneously analyzes seven genes known to cause dominant hereditary ataxias, confirming a clinical diagnosis or assessing carrier status for family planning. فحص لوحة الجينات للكشف عن الطفرات الوراثية للرنح النخاعي المخيخي لسبعة أنواع جينية.
Q: How should I prepare for the blood collection?
No fasting or special preparation is required; a trained phlebotomist draws a small peripheral blood sample using aseptic technique in your home or clinic. لا حاجة للصيام؛ يتم سحب عينة دم وريدية بسيطة بواسطة مختص.
Q: What support will I receive after I get my results?
A DHA‑licensed neurologist will schedule a telephonic consultation to interpret the report, explain pathogenic vs. benign variants, and recommend appropriate management or further genetic counselling. سيقوم طبيب أعصاب مرخص من هيئة الصحة بدبي بتقديم استشارة هاتفية لشرح النتائج.
UAE Regulatory & Quality Compliance
This adheres to Federal Decree-Law No. 41 of 2024 (Art. 87 on diagnostic accuracy and patient rights), the 2026 CDS Law for genetic testing in minors, and UAE PDPL (Federal Decree-Law No. 45 of 2021) for genetic data privacy. Laboratory certified ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139). Facility License: 9834453.
ICD-10-CM 2026 Codes: G11.2 (Late‑onset cerebellar ataxia), G11.1 (Early‑onset cerebellar ataxia), Z13.71 (Encounter for screening for genetic disease carrier status). Additional relevant codes: G11.8, Z84.89. LOINC 86210-1.
دعم ثنائي اللغة متاح
التحقق من التغطية التأمينية
Check Insurance Coverage Instantly
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.
Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians