Test Price
2,800 AED✅ Home Collection Available
THSD1 Gene Thrombospondin Type 1 Domain-Containing Protein 1 Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل الجين THSD1 (بروتين النطاق المحتوي على الثرومبوسبوندين نوع 1) بتقنية التسلسل الجيني عالي الإنتاجية في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
ضمان الدقة بنسبة 99.9% عبر مختبرات حاصلة على شهادة الآيزو 9001:2015، مع خدمة جمع العينات منزلياً بسلسلة تبريد معتمدة.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection and VIP Mobile Phlebotomy (8 AM – 11 PM).
- Clinical Guidance: Complimentary Telephonic Post-Test Clinical Guidance with a DHA-licensed genetic specialist for result interpretation.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview
A comprehensive next-generation sequencing analysis of the entire coding region and splice sites of the THSD1 gene, designed to detect pathogenic variants linked to osteology, dermatology, and immunology disorders. Performed on DNA extracted from blood, FTA card, or extracted DNA sample, this test provides actionable genetic information for precise clinical management.
تحليل جيني شامل لتحديد الطفرات الممرضة في كامل جين THSD1، المرتبطة باضطرابات العظام والجلد والمناعة، مما يوفر تشخيصاً دقيقاً وإرشادات علاجية مخصصة.
| Feature | Our Test (THSD1 Full Gene NGS) | Closest Alternative (Limited Panel/Sanger) |
|---|---|---|
| Precision | 99.9% sensitivity for single nucleotide variants & indels; complete exon coverage | Variable; may miss deep intronic or copy number variants |
| Methodology | Next-Generation Sequencing (NGS) with advanced bioinformatics, aligned to 2026 clinical standards | Sanger sequencing of selected exons or limited hotspot analysis |
| Turnaround Time | 3 to 4 Weeks | Typically 4–6 Weeks (may require multiplex testing) |
Physician Insight & Safety Protocol
“As a DHA-licensed specialist, I understand the emotional weight of genetic testing. A positive result is not a definitive diagnosis, and a negative result does not rule out all hereditary conditions. I strongly recommend that all findings be reviewed with your treating physician to integrate the results into your personal health context.”
— Dr. PRABHAKAR REDDY, DHA License: 61713011
⚠️ Medication Advisory:
Do not discontinue any prescribed medication or alter your treatment plan based on test results without consulting your doctor.
This genetic test is a clinical decision support tool; therapeutic adjustments require a comprehensive medical evaluation.
Exclusion Criteria & Emergency Red Flags
- Exclusion: Patients who have received a whole blood transfusion or undergone stem cell transplantation within the last 4 weeks.
- Exclusion: Immediate post-partum maternal samples without documented consent for infant testing.
- ER Alert: If you experience sudden, unexplained bone pain with swelling, rapid-onset blistering skin lesions, or signs of systemic inflammatory response (fever >38.5°C with rash), seek emergency care immediately.
- Mandatory: A pre-test genetic counselling session is required to draw a pedigree chart and assess family history.
All processing adheres to UAE Federal Decree-Law No. 41 of 2024 (Art. 87), UAE Personal Data Protection Law (PDPL), and CDS Law 2026 for minors. ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139) governs laboratory quality.
Frequently Asked Questions (Clinical Guidance)
1. What conditions can the THSD1 genetic test identify?
This NGS test identifies pathogenic variants in the THSD1 gene directly linked to syndromic disorders affecting bone, skin, and the immune system, enabling targeted interventions.
يحدد تحليل التسلسل الجيني عالي الإنتاجية الطفرات الممرضة في جين THSD1 المرتبطة بمتلازمات تؤثر على العظام والجلد والجهاز المناعي، مما يسمح بتدخلات علاجية موجهة.
2. How is the sample collected and is it painful?
Our VIP home phlebotomy team collects a small blood sample or a single drop on an FTA card; the procedure is quick, virtually painless, and requires no fasting.
يقوم فريق سحب العينات المنزلي بجمع عينة دم صغيرة أو قطرة واحدة على بطاقة FTA؛ الإجراء سريع وغير مؤلم تقريباً ولا يتطلب صياماً.
3. What is the accuracy and TAT of this test?
The delivers 99.9% analytical sensitivity for single nucleotide variants using NGS technology, with a turnaround time of 3–4 weeks from sample receipt.
يحقق الاختبار حساسية تحليلية تبلغ 99.9% للطفرات النقطية باستخدام تقنية التسلسل الجيني عالي الإنتاجية، مع مدة إنجاز تتراوح من 3 إلى 4 أسابيع من استلام العينة.
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التحقق من التغطية التأمينية
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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.
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All reports reviewed by DHA-Certified physicians