Test Price
2,800 AED✅ Home Collection Available
UAE Certified Genetic Testing · ISO 9001:2015 · DHA-Licensed
SPAST Gene (SPG4) Next-Generation Sequencing (NGS) Genetic Test in UAE 2800 AED · 2026 DHA Guidelines
تحليل جين SPAST (SPG4) بتقنية تسلسل الجيل التالي (NGS) في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary & Clinical Safety
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Sequencing and Bioinformatic Validation.
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO-Certified Cold-Chain Transport and VIP Mobile Phlebotomy.
- Clinical Guidance: Complimentary Telephonic Post‑Test Clinical Interpretation with our Senior Neurologist.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731 before collection.
الضمان: دقة تشخيصية بنسبة 99.9% عبر معالجة معتمدة ISO. خدمات لوجستية متميزة: جمع عينات منزلية بجودة المستشفيات عبر سلسلة تبريد معتمدة ISO ونظام سحب دم متنقل VIP. استشارة إكلينيكية هاتفية مجانية بعد ظهور النتائج مع أخصائي الأعصاب.
Compliant with Federal Decree‑Law No. 41 of 2024 (Art. 87), CDS Law 2026 (Minors), and UAE PDPL Data Privacy.
Test Overview
The SPAST Gene SPG4 Genetic Test is a comprehensive analysis designed to detect pathogenic mutations in the SPAST gene, the most common cause of autosomal dominant hereditary spastic paraplegia (HSP‑SPG4). يكشف هذا الفحص الجيني عن الطفرات المسببة للشلل النصفي التشنجي الوراثي من النوع الرابع بدقة عالية. Performed on blood, extracted DNA, or FTA card samples, this test delivers definitive molecular diagnosis with a turnaround time of 3‑4 weeks.
| Feature | Our Test (NGS) | Traditional Sanger Sequencing |
|---|---|---|
| Precision | Full gene coverage, detects single nucleotide variants, indels, and copy number changes | Targeted analysis of known mutations only |
| Method | Next-Generation Sequencing with Sanger confirmation of pathogenic variants | Sanger sequencing of select exons |
| Speed | 3‑4 weeks | 6‑8 weeks |
Physician Insight & Safety Protocol
“At our center, we understand that facing a possible hereditary neurological condition is deeply personal. As a neurologist, I want to reassure you that a positive SPAST result provides clarity and opens the door to targeted management and family planning. However, genetic results must always be correlated with your clinical picture and neurological examination. Please never adjust or discontinue any medication without consulting your physician. We are here to guide you through every step.”
— Dr. Prabhakar Reddy, Senior Neurologist (DHA License No. 61713011)
Medication Warning: Do not discontinue prescribed medication without consulting your doctor.
Patient Safety Exclusion Criteria & Red Flags
- Exclusion Criteria: Individuals under 18 without parental/guardian consent (UAE CDS Law 2026); known acute infection interfering with sample collection; pregnancy for predictive testing must be disclosed.
- Emergency Red Flags: If you experience acute onset of leg paralysis, severe muscle stiffness with inability to walk, or sudden vision loss, seek emergency medical care immediately—this test is not for emergency diagnosis.
Patient FAQ & Clinical Guidance
Q: What is the SPAST gene SPG4 Genetic Test used for?
Our test uses NGS to identify SPAST gene mutations, confirming hereditary spastic paraplegia type 4 diagnosis with 99.9% sensitivity. It helps neurologists differentiate SPG4 from other movement disorders and informs family risk assessment.
اختبار تسلسل الجيل التالي يكشف طفرات جين SPAST لتشخيص الشلل النصفي التشنجي الوراثي SPG4 بدقة.
Q: How is the sample collected for the SPAST gene test?
VIP phlebotomist collects blood or one drop on FTA card at home for genetic testing under strict cold-chain conditions. You can choose a conventional whole blood draw, extracted DNA submission, or a painless finger‑prick FTA card, all handled by our DHA‑licensed mobile team.
جمع العينات يتم عبر خدمة سحب الدم المنزلي باستخدام بطاقة FTA أو عينة دم بسهولة.
Q: What should I do after receiving my SPAST gene test results?
Schedule a telephonic consultation with our neurologist for expert result interpretation and next steps guidance immediately. Together, we will review the clinical significance of any variant found and create a personalized management or family screening plan.
يجب تحديد موعد استشارة هاتفية مع طبيب الأعصاب لتفسير النتائج وتوجيه الخطوات التالية بأسرع وقت.
Pre‑ Requirements:
Clinical history of the patient and a genetic counselling session to draw a pedigree chart of family members affected with SPAST/SPG4 are required before sample collection. No special fasting or medication adjustment is needed. For minors, legal guardian consent is mandatory per UAE CDS Law 2026.
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