Test Price
1,800 AED✅ Home Collection Available
Prader-Willi Syndrome Methylation-Specific PCR Test in UAE | 1800 AED | 2026 DHA Guidelines
تحليل متلازمة برادر-ويلي بتفاعل البوليميراز المتسلسل الخاص بالميثيل في الإمارات | 1800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary
- 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing.
- Hospital-Grade Home Collection: ISO Certified Cold-Chain & VIP Mobile Phlebotomy (Paid).
- Telephonic Post-Test Clinical Guidance in result interpretation.
- Direct Billing Verification: WhatsApp +971 54 548 8731.
الفحص يعتمد على أعلى معايير الجودة وباعتماد هيئة الصحة بدبي، مع ضمان دقة تصل إلى 99.9٪.
Overview
Prader-Willi Syndrome (PWS) is a complex genetic disorder caused by loss of function of paternal genes in chromosome 15q11-q13. This methylation-specific PCR test detects the abnormal methylation pattern to confirm the diagnosis with high precision. In the UAE, this test is guided by 2026 DHA standards and performed on whole blood samples.
ملخص: يستخدم هذا التحليل تقنية PCR الخاص بالميثيل لتأكيد متلازمة برادر-ويلي عبر كشف نمط الميثيل غير الطبيعي.
| Aspect | Our Test | Alternative (e.g., FISH) |
|---|---|---|
| Precision | >99% methylation detection | ~85% for deletion detection |
| Methodology | Methylation-Specific PCR (MS-PCR) | Fluorescence in situ hybridization (FISH) |
| Turnaround Time | 12 Working Days | 10-14 Days |
Physician Insight & Safety Protocol
Dr. Prabhakar Reddy (DHA: 61713011): “While this methylation-specific PCR test is highly accurate, clinical correlation with growth, developmental milestones, and genetic counseling remains essential. No molecular test replaces comprehensive pediatric evaluation.”
“Please do not discontinue any prescribed medication or therapy without consulting your treating physician. The results must be interpreted in the broader clinical context.”
⚠️ Important Medication Warning:
Do not discontinue prescribed medication (e.g., growth hormone, thyroid supplements, antiepileptics) without consulting your doctor. Abrupt changes can lead to serious health risks in PWS patients.
Exclusion Criteria & Emergency Red Flags
- Sample unsuitable if not refrigerated; do not freeze. Hemolyzed or clotted blood will be rejected.
- Incomplete or missing Genomics Clinical Information Requisition Form (Form 20) will delay testing.
- Seek ER immediately if child develops severe hypotonia, feeding difficulties, or respiratory distress; these are not test-related but indicate urgent PWS complications.
Patient FAQ & Clinical Guidance
What does the Prader-Willi methylation test detect, and how accurate is it?
This directly identifies abnormal methylation patterns at chromosome 15q11-q13 with 99.9% diagnostic sensitivity, confirming PWS in over 99% of typical cases.
ما هو الوقت المتوقع لظهور نتائج فحص متلازمة برادر-ويلي؟
تصدر النتيجة في غضون 12 يوم عمل من استلام العينة، مع إمكانية الإبلاغ عبر تطبيق واتساب أو البوابة الإلكترونية.
Is home blood collection available for children in Dubai or Abu Dhabi?
Yes, our VIP hospital-grade home collection service covers all Emirates with specially trained pediatric phlebotomists, ensuring minimal discomfort and cold-chain transport.
This service complies with Federal Decree-Law No. 41 of 2024 (Art. 87), UAE PDPL, and Child Data Sensitivity Law 2026. Laboratory licensed under Facility No. 9834453, ISO 9001:2015 Certified (Cert: INT/EGQ/2509DA/3139).
All medical interpretations are provided by DHA-certified clinicians. This content is for informational purposes and does not constitute medical advice. Consult your physician.
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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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ISMS 27001:2022
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All reports reviewed by DHA-Certified physicians