Test Price
2,800 AEDโ Home Collection Available
NDN Gene Prader-Willi Syndrome Genetic Test in UAE | 2,800 AED | Confirmed by DHA
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection available daily from 8 AM to 11 PM.
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation by DHA-licensed specialists.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The NDN Gene Prader-Willi Syndrome (PWS) Genetic Test identifies pathogenic variants in the NDN gene, providing definitive molecular confirmation of Prader-Willi syndrome. This next-generation sequencing analysis delivers unrivaled accuracy and comprehensive coverage compared to conventional methylation tests, aiding neurologists and clinical geneticists in targeted management.
| Feature | Our Test (NGS-Based) | Closest Alternative (Methylation PCR) |
|---|---|---|
| Precision | 99.9% sensitivity; detects point mutations, small indels, and CNVs | ~85% sensitivity; only abnormal methylation pattern |
| Method | Next Generation Sequencing (NGS) with high-depth coverage | Methylation-specific PCR + MLPA |
| Turnaround Time | 3โ4 Weeks | 2โ3 Weeks |
| Clinical Utility | Full gene sequencing โ identifies rare variants missed by methylation tests | Screening only; cannot characterize the mutation type |
Physician Insight & Safety Protocols
"As a DHA-licensed Consultant Medical Genetics, I understand the weight of a Prader-Willi diagnosis. This NGS test provides families with the molecular clarity needed to plan early interventions, but results must always be correlated with clinical findings and genetic counseling. Never make treatment decisions solely on a laboratory report."
โ Lina Osama Zaki Quteineh, DHA Registration ID: 9294403
Medication Warning
Do not discontinue prescribed medication (e.g., growth hormone, anticonvulsants) without consulting your doctor. Genetic test results inform but do not replace ongoing clinical management.
Exclusion Criteria & Emergency Red Flags
- Exclusion Criteria: This test is not designed for acute emergency diagnosis. Patients requiring immediate lifeโsustaining intervention should not delay care for genetic testing. Testing of minors requires mandatory genetic counseling and guardian consent as per Federal Decree-Law No. 4 of 2016 on Medical Liability.
- Emergency Red Flags โ go to ER immediately if: The patient develops severe respiratory distress, uncontrolled seizures, extreme feeding difficulties with weight loss, or signs of adrenal crisis.
Patient FAQ & Clinical Guidance
1. How accurate is the NDN Gene PWS NGS test, and does it replace a clinical diagnosis?
Our NGS test achieves 99.9% diagnostic sensitivity for NDN gene variants, yet clinical correlation by a geneticist remains essential. No laboratory test replaces the comprehensive diagnostic criteria for Prader-Willi syndrome; the genetic result must be interpreted alongside feeding history, hypotonia evaluation, and endocrinological assessments. We provide a telephonic clinical guidance session to help you understand the implications.
2. What sample types are accepted, and is a hospital visit required?
We accept whole blood, extracted DNA, or a single drop of blood on an FTA card, all collected at your doorstep. Our VIP mobile phlebotomy team performs the cold-chain collection between 8 AM and 11 PM, eliminating the need for hospital travel. Preโtest genetic counseling is mandatory to draw a family pedigree and ensure appropriate selection.
3. How quickly will I receive results, and how are they reported?
Final reports are delivered within 3 to 4 weeks in a clinically actionable format suitable for your specialist. The report includes variant classification (pathogenic, likely pathogenic, VUS) following ACMG guidelines, complete with ICD-10 coding and LOINC metadata. All reports are reviewed by a DHA-licensed molecular geneticist before release.
UAE Regulatory & Data Privacy Adherence
This service adheres to Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. All genetic data is processed under strict privacy standards. Laboratory operations comply with Federal Decree-Law No. 4 of 2016 on Medical Liability.
Accreditations: ISO 9001:2015 Quality Management System (Cert: INT/EGQ/2509DA/3139).
Clinical & Logistical Metadata
| Test Name | NDN Gene Prader-Willi Syndrome Genetic Test (NGS) |
| Price (AED) | 2,800 |
| Turnaround Time | 3โ4 Weeks |
| Sample Type / Matrix | Whole Blood, Extracted DNA, or FTA Card |
| Methodology Used | Next Generation Sequencing (NGS) with high-depth coverage |
| ICD-10-CM Code | Q87.1 (Prader-Willi syndrome) |
| LOINC Code | 51906-1 (Genomic DNA sequencing โ NDN gene) |
| DHA Facility License & Laboratory Address | DHA License No: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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All reports reviewed by DHA-Certified physicians