Test Price
3,100 AED✅ Home Collection Available
Tuberous Sclerosis Complex (TSC) Genetic Testing in UAE | 3100 AED | 2026 DHA Guidelines
تحليل الفحص الجيني للتصلب الحدبي المركب (TSC) في الإمارات | 3100 درهم | معتمد من هيئة الصحة بدبي
ملخص تنفيذي: تحليل جيني دقيق ومعتمد لتشخيص التصلب الحدبي المركب مع خدمة سحب الدم المنزلي والاستشارة الطبية بعد الفحص.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing.
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection and VIP Mobile Phlebotomy.
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Overview
The Tuberous Sclerosis Complex (TSC) Genetic Testing panel uses Next‑Generation Sequencing (NGS) with Sanger confirmation to detect pathogenic variants in TSC1 and TSC2 genes with over 99.9% diagnostic sensitivity. في هذا التحليل الجيني المتقدم، نستخدم التسلسل من الجيل التالي مع تأكيد سانغر لتشخيص التصلب الحدبي المركب بدقة متناهية.
| Feature | Our Test (NGS + Sanger) | Closest Alternative (PCR + Sanger) |
|---|---|---|
| Methodology | NGS with full gene coverage & Sanger confirmation | Targeted PCR for common hotspots & Sanger |
| Sensitivity | 99.9% (detects SNVs, indels, CNVs) | ~85% (limited to known mutations) |
| Turnaround Time | 30 days | 4–8 weeks |
| Price | 3,100 AED | Not directly comparable |
| Gene Coverage | Complete TSC1 & TSC2 coding regions | Partial exon analysis only |
Physician Insight & Safety Protocol
Dr. PRABHAKAR REDDY (DHA License: 61713011), Consultant Neurologist, shares: “Genetic testing for TSC yields the most clinical value when integrated with a thorough neurological exam and family history. A negative result does not rule out TSC if physical criteria are met; I always correlate molecular data with imaging and clinical signs. This test empowers families to understand recurrence risk and access early intervention, but it is not a substitute for ongoing specialist care.”
Medication Warning: Do not discontinue prescribed medication without consulting your doctor.
Exclusion Criteria & Emergency Red Flags
- Minors: Testing for individuals under 18 years requires documented guardian consent per UAE CDS Law 2026.
- Sample Rejection: Hemolyzed, clotted, or frozen-thawed blood; incomplete Clinical Exome Testing Requisition Form (Form 36).
- ER Red Flags: Seizure lasting longer than 5 minutes, sudden vision loss, severe headache with vomiting, or acute developmental regression – seek emergency care immediately.
- Pregnancy/Lactation: Not a contraindication, but clinical urgency should be discussed with your ordering physician.
Patient FAQ & Clinical Guidance
What is the purpose of TSC genetic testing?
TSC genetic testing identifies mutations in TSC1/TSC2 genes to confirm diagnosis and guide family risk assessment. يقوم التحليل الجيني لتصلب الحدبي المركب بتحديد الطفرات في جينات TSC1 وTSC2 لتأكيد التشخيص وتقييم المخاطر العائلية. The test is recommended when clinical criteria are suspected, for prenatal counseling, or to determine eligibility for mTOR inhibitor therapy.
How should I prepare for the test?
No fasting required; simply ensure the Clinical Exome Testing Requisition Form (Form 36) is fully completed. لا يتطلب التحليل صيامًا؛ فقط تأكد من تعبئة نموذج طلب فحص الإكسوم السريري (نموذج 36) بالكامل. Our phlebotomist will collect 10 mL of blood in two lavender‑top EDTA tubes, strictly refrigerated during transport.
How long does it take to receive results?
Reports are typically delivered within 30 working days after sample receipt due to complex sequencing and interpretation. تُسلم التقارير عادةً خلال 30 يوم عمل من استلام العينة، نظراً لدقة التسلسل الجيني وتفسير النتائج. You will be notified via SMS and can schedule a post‑ consultation with Dr. Reddy at no additional cost.
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