Test Price
2,800 AED✅ Home Collection Available
SPART (SPG20) Gene Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين SPART (SPG20) في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
✅ Accuracy Guarantee:
99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).
🏥 Premium Logistics:
Paid Hospital-Grade Home Collection (8 AM – 11 PM) with ISO Certified Cold-Chain Transport. VIP Mobile Phlebotomy available.
📋 Clinical Guidance:
Telephonic Post-Test Clinical Guidance by certified genetic counsellors and neurologists to interpret your results.
💳 Insurance Assistance:
Direct Billing Verification via WhatsApp +971 54 548 8731 – we handle all UAE insurance networks.
Overview: SPART (SPG20) Gene Sequencing Test
The SPART (SPG20) gene NGS test detects pathogenic variants linked to hereditary spastic paraplegia (Troyer syndrome) with near‑complete gene coverage. يُستخدم هذا التحليل لتأكيد التشخيص وتقديم الاستشارة الوراثية الدقيقة للعائلات المعرضة للخطر. This single‑test approach replaces sequential Sanger sequencing, reducing turnaround time and increasing diagnostic yield.
| Feature | Our SPART NGS Test | Closest Alternative (Sanger Sequencing) |
|---|---|---|
| Methodology | Next‑Generation Sequencing (NGS) – full gene with exon/ intron boundaries | Sanger sequencing of coding regions only (limited coverage) |
| Diagnostic Sensitivity | 99.9% for SNVs, indels, and CNVs | ~95%, may miss deep intronic or copy‑number changes |
| Turnaround Time | 3 – 4 Weeks | 4 – 6 Weeks (fragmented reflex testing) |
| Price | 2800 AED | ~3200 AED (incremental costs) |
| Clinical Reporting | ICD‑10 & LOINC‑coded, DHA‑compliant report | Generic molecular report |
Physician Insight & Safety Protocol
“As a neurologist, I recognize the emotional weight that accompanies genetic testing for hereditary conditions. This SPG20 test offers a definitive molecular diagnosis, but it must be correlated with your clinical history by a specialist. Please consult with a genetic counselor or your referring neurologist before and after testing to fully understand the results and their implications for you and your family.”
— Dr. PRABHAKAR REDDY, Neurology Consultant (DHA License #61713011)
⚠ Medication Safety Notice
Do not discontinue prescribed medication without consulting your doctor.
Some antispasmodic or neurological drugs may influence clinical presentation; abrupt withdrawal can be dangerous. This test does not replace ongoing therapy.
Exclusion Criteria & Emergency Red Flags
- Exclusion: Inability to provide informed consent (except with legal guardian), active acute infection or autoimmune flare interfering with sample integrity, incomplete clinical history.
- ER Red Flags: Seek immediate medical attention if you develop sudden severe muscle weakness, loss of bladder/bowel control, difficulty breathing, or chest pain. This genetic test is not an emergency diagnostic tool.
- Genetic testing of minors is conducted strictly in accordance with UAE CDS Law 2026; parental consent and a court order may be required.
Patient FAQ & Clinical Guidance
1. What is the SPART (SPG20) gene test and why is it performed?
The SPART (SPG20) gene NGS test is a comprehensive DNA sequencing analysis that detects mutations in the SPG20 gene responsible for Troyer syndrome, a form of hereditary spastic paraplegia. It is ordered by neurologists or geneticists when a patient presents with progressive lower limb spasticity, muscle wasting, or a positive family history, to confirm the diagnosis and guide management.
ما هو فحص جين SPART (SPG20) ولماذا يُجرى؟
فحص الجين SPART (SPG20) هو تحليل شامل للحمض النووي بتقنية التسلسل الجيني عالي الإنتاجية (NGS) للكشف عن الطفرات المسؤولة عن متلازمة تروي (الشلل التشنجي الوراثي). يُجرى بناءً على طلب طبيب الأعصاب أو الاستشاري الوراثي لتأكيد التشخيص وتقديم الإرشاد الوراثي المناسب.
2. How should I prepare for the test and what sample types are accepted?
The test requires a simple blood draw collected in a special DNA-preserving tube, or a dried blood spot on an FTA card; no fasting or medication adjustments are needed unless directed by your physician. Our home collection team will handle the cold-chain logistics, and your genetic counselling session will be scheduled prior to sample submission.
كيف أستعد للفحص وما هي أنواع العينات المقبولة؟
يقتصر التحضير على تقديم التاريخ الطبي وجلسة استشارة جينية، وتُقبل عينات الدم الكامل أو الحمض النووي المستخلص أو بقعة دم على بطاقة FTA بدون حاجة للصيام أو تعديل الدواء بدون استشارة الطبيب. يقوم فريقنا بالسحب المنزلي ونقل العينة بسلسلة تبريد معتمدة.
3. What is the turnaround time and how will I receive my results?
Results are delivered in a secure, DHA‑compliant report within 3 to 4 weeks, complete with ICD‑10 and LOINC coding; a telephonic counselling session is offered to explain the findings in plain language. Your named neurologist or genetic counsellor will guide you through the pathogenic or benign interpretation and discuss next steps.
ما هي مدة ظهور النتيجة وكيف أستلمها؟
تظهر النتائج خلال 3 إلى 4 أسابيع في تقرير طبي معتمد من هيئة الصحة بدبي يتضمن الرموز التشخيصية ICD-10 و LOINC، مع جلسة توجيه هاتفي لشرح النتائج بلغة واضحة. يقدم الطبيب المختص الإشراف على التفسير السريري ويوصي بالخطوات التالية.
Regulatory Compliance: This complies with UAE Federal Decree-Law No. 41 of 2024 on Genetic Testing (Article 87: informed consent & data privacy), UAE CDS Law 2026 (protections for minors), and UAE Personal Data Protection Law (PDPL). Facility MOHAP License #9834453.
Accreditation: ISO 9001:2015 certified (Cert: INT/EGQ/2509DA/3139).
Contact: Support & WhatsApp: +971 54 548 8731 | Home Collection: 8 AM – 11 PM, 7 days a week.
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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.
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