Test Price
2,800 AED✅ Home Collection Available
SAR1B Gene (Chylomicron Retention Disease) Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين SAR1B (مرض احتباس الكيلومكرونات) في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary
99.9% Diagnostic Sensitivity via ISO 15189-accredited NGS laboratory. This test definitively detects variants in the SAR1B gene associated with chylomicron retention disease (Anderson disease), ensuring accurate diagnosis and family risk assessment under 2026 DHA guidelines. ملخص تنفيذي: ضمان دقة تشخيصية بنسبة 99.9% عبر التحليل الجيني المتقدم وفقًا لتوجيهات هيئة الصحة بدبي لعام 2026.
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection and VIP Mobile Phlebotomy (8 AM – 11 PM).
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Overview
The SAR1B gene test uses Next-Generation Sequencing to identify disease-causing mutations responsible for chylomicron retention disease—a rare metabolic disorder characterized by failure to export dietary fats from enterocytes. This test is essential for confirming clinical suspicion, guiding dietary management, and enabling cascade screening of at-risk relatives.
| Feature | Our Test (NGS) | Closest Alternative (Sanger Sequencing) |
|---|---|---|
| Methodology | Targeted NGS with 99.9% sensitivity | Sanger sequencing, lower variant coverage |
| Turnaround Time | 3–4 Weeks | 4–6 Weeks |
| Variant Detection | SNVs, INDELs, CNVs across full gene | Limited to known hotspots |
*Price: 2800 AED. Sample Type: Blood, extracted DNA, or one drop of blood on FTA Card. TAT: 3 to 4 weeks.
Physician Insight & Safety Protocol
“As a clinician, I emphasize that a positive SAR1B result must be correlated with clinical findings such as failure to thrive, steatorrhea, and hypocholesterolemia. This genetic diagnosis empowers families with precise nutritional strategies and prevents unnecessary interventions. Always consider variant reclassification over time.” — Dr. PRABHAKAR REDDY (DHA: 61713011)
Medication Warning
Do not discontinue prescribed medication or lipid-modifying therapies without consulting your doctor.
Exclusion Criteria: Acute infection, recent transfusion (<2 weeks), or anticoagulant therapy that contraindicates blood draw. ER Red Flags: Severe malnutrition, gastrointestinal bleeding, or neurological deterioration in a suspected patient require urgent evaluation before genetic testing.
Pre-Test Requirement: Clinical history intake and a genetic counselling session to draw a pedigree chart of family members affected by chylomicron retention disease are mandatory. Avoid supplements or drugs that interfere with lipid metabolism; a full list will be provided during the pre-test consultation.
Patient FAQ & Clinical Guidance
Q1: How accurate is this SAR1B genetic test for diagnosing chylomicron retention disease?
Our NGS-based test achieves diagnostic accuracy exceeding 99.9% for detecting pathogenic variants in the SAR1B gene, far surpassing traditional biochemical assays or single-gene sequencing. This high sensitivity is validated through ISO 15189-accredited protocols and 2026 DHA guidelines, making it the most reliable genetic confirmation tool available in the UAE.
السؤال: ما مدى دقة هذا الاختبار الجيني لمرض احتباس الكيلومكرونات؟ الجواب: تصل دقة الاختبار القائم على التسلسل الجيني من الجيل التالي إلى أكثر من 99.9% في كشف الطفرات المسببة للمرض، وهو ما يفوق الطرق التقليدية.
Q2: Can I do the test at home, and how is the sample collected?
Yes, we provide paid hospital-grade home collection with cold-chain transport; a certified phlebotomist visits your location between 8 AM and 11 PM, collecting either a standard blood sample or a simple finger-prick FTA card, ensuring DNA stability until analysis.
السؤال: هل يمكن إجراء الفحص في المنزل؟ الجواب: نعم، نوفر خدمة سحب منزلي معتمدة بتقنية سلسلة التبريد مع فريق تمريض مرخص، ويمكنكم استخدام بطاقة FTA أو عينة دم عادية.
Q3: What turnaround time can I expect, and is insurance coverage available?
Results are delivered within 3 to 4 weeks, and our dedicated insurance team will verify direct billing via WhatsApp before the, ensuring coverage alignment with your policy and UAE federal regulations.
السؤال: ما مدة ظهور النتيجة وهل يشمل التأمين؟ الجواب: تصدر النتائج خلال 3 إلى 4 أسابيع، ويتم التحقق من تغطية التأمين عبر الواتساب قبل الفحص.
Legal Compliance: This service adheres to UAE Federal Decree-Law No. 41 of 2024 (Art. 87), the CDS Law 2026 regarding minors, and UAE PDPL for data privacy. ISO 9001:2015 certification (Cert: INT/EGQ/2509DA/3139). Facility License: 9834453.
Support: Phone/WhatsApp +971 54 548 8731. All content is clinically reviewed by DHA-licensed physician Dr. PRABHAKAR REDDY (61713011).
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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.
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All reports reviewed by DHA-Certified physicians