Test Price
3,000 AED✅ Home Collection Available
MPS Enzyme Panel (Genetic Test) in UAE | 3000 AED | 2026 DHA Guidelines
تحليل لوحة إنزيم MPS (فحص الحمض النووي الجيني NGS) في الإمارات | 3000 درهم | معتمد من هيئة الصحة بدبي
Executive Summary | ملخص تنفيذي
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity achieved through ISO 9001:2015 accredited NGS processing and variant confirmation by Sanger sequencing. ضمان الدقة: حساسية تشخيصية بنسبة 99.9% عبر معالجة بتقنية NGS معتمدة من ISO وتأكيد الطفرات بتسلسل سانجر.
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection and VIP Mobile Phlebotomy service available 8 AM – 11 PM daily.
- Clinical Guidance: Inclusive post-test telephonic clinical guidance with an expert genetic counsellor for result interpretation and family risk assessment.
- Insurance: Direct Billing Verification via WhatsApp at +971 54 548 8731. We handle pre-approval with leading UAE insurers.
Test Overview
This advanced MPS Enzyme Panel Genetic Test analyses the entire coding regions of genes associated with Mucopolysaccharidoses (MPS) – a group of inherited lysosomal storage disorders. Using next-generation sequencing on a single blood, DNA, or dried blood spot sample, it identifies pathogenic variants that cause enzyme deficiencies, enabling early diagnosis and personalised management. يقدم هذا الفحص الجيني المتطور تحليلاً شاملاً للجينات المرتبطة بداء عديد السكاريد المخاطي (MPS) من خلال عينة دم أو بطاقة FTA، مما يتيح التشخيص المبكر والإدارة العلاجية الموجهة.
| Feature | Our Test (ISO 9001:2015) | Closest Alternative |
|---|---|---|
| Precision | 99.9% Diagnostic Sensitivity, Sanger confirmation | Enzyme activity assay (may miss carrier status) |
| Method | NGS (Illumina platform) + bioinformatic analysis | Biochemical enzyme assay or single-gene sequencing |
| Turnaround | 3–4 weeks | 4–6 weeks for similar panel |
Physician Insight & Safety Protocol
Dr. PRABHAKAR REDDY (DHA License: 61713011) advises: “This NGS panel is a powerful tool for identifying MPS at the molecular level, but results must be correlated with clinical symptoms and enzyme activity. A negative report does not completely exclude all metabolic disorders, and a positive finding should be discussed in a genetic counselling session to understand inheritance and family implications. Please continue any current enzyme replacement therapy or symptom management until your specialist reviews the genetic data.”
Medication Warning
Do not discontinue prescribed medication without consulting your doctor. Genetic results provide risk information, not a substitute for ongoing clinical care.
Exclusion Criteria & Emergency Red Flags
- Exclusion: Inability to provide a blood sample or DNA specimen; recent bone marrow transplant (may cause mixed chimerism affecting DNA analysis).
- Exclusion: Unconfirmed clinical suspicion of MPS; test is not a first-line screening for asymptomatic individuals without family history or metabolic symptoms.
- Red Flag – Seek immediate medical care: Acute metabolic decompensation, severe vomiting, hypotonia, or loss of consciousness. Go to the nearest Emergency Department.
- Red Flag: Rapid progression of neurological deterioration in a child already diagnosed; test should not delay urgent enzyme replacement therapy or supportive care.
Frequently Asked Questions
Q1: How accurate is the MPS Enzyme Panel NGS test for diagnosing mucopolysaccharidosis?
س1: ما مدى دقة فحص لوحة إنزيم MPS بتقنية NGS في تشخيص داء عديد السكاريد المخاطي؟
A: With 99.9% diagnostic sensitivity and Sanger confirmation, this NGS panel provides the gold standard in genetic diagnosis of MPS. It detects single nucleotide variants, small indels, and copy number variations across all targeted genes. False negatives are minimised by deep sequencing coverage, but a negative result cannot exclude rare deep intronic variants. يوفر هذا الفحص المعيار الذهبي للتشخيص الجيني لداء MPS بحساسية 99.9% وتأكيد بتسلسل سانجر، ويكشف عن الطفرات النقطية والإدراج والحذف والتغيرات في عدد النسخ.
Q2: What sample is required and how is the home collection performed?
س2: ما العينة المطلوبة وكيف يتم سحبها منزلياً؟
A: A simple blood draw, one drop of blood on an FTA card, or previously extracted DNA can be used, collected from home by our VIP mobile phlebotomy team. Our ISO-certified cold-chain logistics ensure sample stability from your doorstep to the lab within 4 hours. The courier carries a validated transport kit, and the procedure takes less than 10 minutes. يمكن استخدام عينة دم وريدي أو قطرة دم على بطاقة FTA أو حمض نووي مستخلص، ويقوم فريقنا المتنقل بسحب العينة منزلياً وفق معايير النقل المبرد المعتمدة خلال 4 ساعات.
Q3: Is this test covered by UAE health insurance, and how to verify?
س3: هل يغطي التأمين الصحي هذا الفحص في الإمارات وكيف يمكن التحقق؟
A: Most UAE insurers cover this when medically necessary; our billing team provides direct verification via WhatsApp at +971545488731 before the draw. We require a referral from a DHA-licensed physician and pre-authorisation code. Please send a copy of your insurance card and Emirates ID to the same number for a prompt eligibility check. تغطي معظم شركات التأمين في الإمارات هذا الفحص عند الحاجة الطبية، ويقوم فريق الفوترة بالتحقق الفوري عبر واتساب برقم +971545488731 قبل سحب العينة بعد استلام الإحالة وصورة الهوية.
Compliant with UAE Federal Decree-Law No. 41 of 2024 (Art. 87), CDS Law 2026 (Minors), and UAE PDPL. ISO 9001:2015 Certified (Cert: INT/EGQ/2509DA/3139). Laboratory Facility License: 9834453. Methodologies follow 2026 AI-validated NGS protocols (LC-MS/MS where applicable). This page is reviewed by DHA-licensed clinical experts.
ICD-10-CM codes: E76.0, E76.1, E76.2. LOINC: 81960-4 (Lysosomal storage disease multigene panel).
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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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