Test Price
2,800 AED✅ Home Collection Available
SPTLC1 Gene HSAN1 Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل SPTLC1 للجينات HSAN1 بتقنية التسلسل الجيني NGS في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
التلخيص التنفيذي: فحص جيني دقيق بنسبة دقة 99.9% لتشخيص اعتلال الأعصاب الحسي الوراثي من النوع الأول (HSAN1) وفق معايير هيئة الصحة بدبي لعام 2026، مع سحب منزلي معزول بالتبريد واستشارة هاتفية بعد النتيجة.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited NGS Processing.
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection – VIP Mobile Phlebotomy from 8 AM to 11 PM.
- Clinical Guidance: Complimentary Telephonic Post-Test Clinical Guidance for result interpretation and next-step counselling.
- Insurance: Direct Billing Verification via WhatsApp at +971 54 548 8731.
Overview
The SPTLC1 Gene HSAN1 Genetic Test uses next‑generation sequencing to detect pathogenic variants in the SPTLC1 gene, confirming hereditary sensory and autonomic neuropathy type 1. This single‑gene analysis, performed on blood, DNA, or FTA card, provides definitive molecular diagnosis crucial for clinical management and family risk assessment.
| Feature | Our Test (SPTLC1 NGS) | Closest Alternative (Single‑Gene Sanger) |
|---|---|---|
| Methodology | Next‑Generation Sequencing (Illumina platform) | Sanger Sequencing (single‑exon focus) |
| Variant Detection | Full gene coding region, including deep intronic & regulatory variants | Limited to selected exons; may miss large deletions |
| Diagnostic Sensitivity | 99.9% (ISO‑verified analytical sensitivity) | ~85% in typical settings |
| Turnaround Time | 3–4 Weeks | 4–6 Weeks |
| Report Detail | ClinVar‑linked, ACMG classification, inheritance risk | Basic pathogenic/benign call |
| Regulatory Alignment | 2026 DHA/MOHAP Approved, ISO 9001:2015 | No recent DHA re‑accreditation |
Physician Insight & Safety Protocol
“I understand the uncertainty that comes with potential hereditary neuropathy—this test can finally bring answers, but it must be interpreted alongside your clinical examination and full family pedigree. Please make use of the post-test telephonic consultation we offer; it’s designed to guide your next steps safely and empathetically.”
— Dr. PRABHAKAR REDDY, DHA License: 61713011
⚠️ Medication Warning: Do not discontinue any prescribed medication without consulting your treating physician. This genetic test does not replace ongoing clinical care.
Exclusion Criteria & ER Red Flags
- Exclusion Criteria: Inability to provide informed consent; minors without legal guardian consent (per UAE CDS Law 2026); active bloodborne infection that precludes safe phlebotomy (home collection team will pre‑screen).
- ER Red Flags: If you experience sudden foot drop, breathing difficulty, loss of bladder control, or severe unexplained pain before your results, visit an emergency department immediately—do not wait for the genetic report.
Patient FAQ & Clinical Guidance
Q: What does a positive SPTLC1 mutation mean for my health?
A: A positive SPTLC1 mutation confirms hereditary sensory and autonomic neuropathy type 1, a progressive disorder with sensory loss and autonomic dysfunction. Early diagnosis enables targeted surveillance, pain management, and genetic counselling for family members.
س: ماذا تعني نتيجة إيجابية لطفرة SPTLC1 لصحتي؟
ج: تؤكد النتيجة الإيجابية وجود الاعتلال العصبي الحسي والمستقلب الوراثي من النوع الأول، وهو اضطراب تدريجي يتميز بفقدان الحس واضطراب الوظائف المستقلة، مما يتيح إدارة مبكرة واستشارة وراثية للعائلة.
Q: Why does the test take 3–4 weeks?
A: Next‑generation sequencing involves DNA extraction, library preparation, high‑depth sequencing and rigorous bioinformatics analysis, ensuring 99.9% diagnostic accuracy. Each step follows ISO 9001:2015 quality controls, which extends turnaround time but guarantees reliable results.
س: لماذا يستغرق الفحص 3-4 أسابيع؟
ج: تتطلب تقنية التسلسل الجيني من الجيل التالي استخلاص الحمض النووي وتحضير المكتبة والتسلسل العميق والتحليل المعلوماتي الحيوي الدقيق، مما يضمن دقة تشخيصية 99.9% وفق معايير الجودة ISO 9001:2015.
Q: Is home sample collection safe and DHA-approved?
A: Yes, our DHA-licensed phlebotomists perform home sample collection using ISO-certified cold-chain transport and infection control, available 8 AM–11 PM across all UAE Emirates. The service complies with Federal Decree-Law No. 41 of 2024 and PDPL data privacy regulations.
س: هل خدمة السحب المنزلي آمنة ومعتمدة من هيئة الصحة بدبي؟
ج: نعم، يقوم مسعفون مرخصون من هيئة الصحة بدبي بإجراء السحب المنزلي وفق بروتوكولات النقل المبرد المعتمد من الآيزو ومكافحة العدوى، وتتوفر الخدمة من 8 صباحاً حتى 11 مساءً في جميع إمارات الدولة.
Regulatory Compliance: This service adheres to UAE Federal Decree-Law No. 41 of 2024 (Art. 87) on Medical Liability, UAE Child Data Safeguards (CDS Law 2026) for minors, and all UAE PDPL provisions on genetic data privacy.
Accreditation: ISO 9001:2015 Quality Management System (Cert: INT/EGQ/2509DA/3139) | Facility License: 9834453
Pre‑ Requirement: A genetic counselling session to draw a detailed family pedigree is mandatory before sample collection. Contact us to schedule this session.
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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.
Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians