Test Price
2,800 AED✅ Home Collection Available
SCP2 Gene Leukoencephalopathy with Dystonia and Motor Neuropathy Genetic Test (NGS) in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين SCP2 لمرض الاعتلال الأبيض الدماغي مع خلل التوتر والاعتلال العصبي الحركي في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
الخلاصة التنفيذية: دقة تشخيصية 99.9% وخدمة منزلية فاخرة
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Certified Laboratory (Cert: INT/EGQ/2509DA/3139) employing validated NGS methodology.
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection, VIP Mobile Phlebotomy (8:00 AM – 11:00 PM).
- Clinical Guidance: Telephonic Post-Test Clinical Guidance for result interpretation with DHA-licensed specialists (DHA: 61713011).
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology Comparison
The SCP2 Gene Leukoencephalopathy with Dystonia and Motor Neuropathy Genetic Test employs high-coverage Next Generation Sequencing to detect pathogenic variants in the entire SCP2 gene, enabling definitive diagnosis of this rare neurometabolic disorder. اختبار جيني متقدم للكشف عن الطفرات المسببة للاعتلال الأبيض الدماغي مع خلل التوتر والاعتلال العصبي الحركي بدقة عالية.
| Feature | Our NGS Test (SCP2 Gene) | Alternative (Sanger Sequencing) |
|---|---|---|
| Coverage | Full gene including introns & regulatory regions | Selected coding exons only |
| Analytical Sensitivity | >99.9% | ~95% |
| Turnaround Time | 3–4 Weeks | 6–8 Weeks |
| Accreditation | ISO 9001:2015 (INT/EGQ/2509DA/3139) | May vary |
Physician Insight & Safety Protocol
“As a DHA-licensed neurologist, I emphasize that this NGS test is critical for confirming SCP2-related leukoencephalopathy; however, results must be correlated with clinical presentation and neuroimaging. Genetic counseling prior to testing is non-negotiable to interpret findings accurately.”
— Dr. Prabhakar Reddy, DHA License No. 61713011
Medication Warning
Do not discontinue prescribed medication without consulting your doctor.
Exclusion Criteria & Emergency Red Flags
- Patients who have not undergone pre-test genetic counseling and pedigree analysis.
- Inadequate clinical documentation of neurological symptoms (hypotonia, dystonia, motor regression).
- Emergency Red Flags: If you experience sudden severe dystonic crisis, respiratory difficulty, or loss of consciousness, seek immediate medical attention at the nearest ER.
Patient FAQ & Clinical Guidance
Why is the SCP2 gene test preferred over whole exome sequencing for this condition?
Our comprehensive NGS test confirms SCP2-related leukoencephalopathy with dystonia and motor neuropathy with superior diagnostic accuracy. Unlike whole exome sequencing, this focused assay provides deep coverage of the entire SCP2 gene, capturing both coding and non-coding pathogenic variants, and delivers results in 3–4 weeks with ISO-accredited quality control.
هل يتطلب هذا الفحص استشارة وراثية مسبقة؟
يتطلب هذا الفحص الجيني استشارة وراثية إلزامية لرسم شجرة العائلة وتحديد المخاطر الموروثة بدقة. يجب إجراء جلسة استشارة وراثية قبل الفحص لمناقشة التاريخ العائلي وتوثيق الأعراض السريرية لضمان تفسير دقيق للنتائج.
What should I do if my result is positive?
Positive result confirms SCP2 leukoencephalopathy with dystonia and motor neuropathy; need neurology follow-up and family counseling. Your DHA-licensed neurologist will interpret the result in context of clinical symptoms and arrange genetic counseling for at-risk relatives.
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Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians