Test Price
2,800 AED✅ Home Collection Available
LIPA Gene Sequencing for Wolman Disease (NGS) in UAE – 2800 AED – Molecular Diagnosis
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 accredited processing.
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (daily 8 AM – 11 PM).
- Clinical Guidance: Telephonic Post‑Test Clinical Guidance on result interpretation included.
- Insurance: Direct Billing Verification via WhatsApp at +971 54 548 8731.
Test Overview & Methodology
The LIPA Gene Sequencing for Wolman Disease uses Next‑Generation Sequencing (NGS) to detect pathogenic variants in the LIPA gene, confirming lysosomal acid lipase deficiency – a severe metabolic disorder presenting in infancy. Our test delivers definitive molecular diagnosis with full gene coverage and copy number variation (CNV) detection, achieving 99.9% sensitivity.
| Feature | Our Test (NGS) | Closest Alternative (Sanger) |
|---|---|---|
| Precision | Full gene coverage, CNV detection | Limited hotspot sequencing |
| Methodology | NGS + bioinformatics (LC‑MS/MS validation) | Sanger sequencing only |
| Turnaround | 3 – 4 Weeks | 4 – 6 Weeks |
Physician Insight & Safety Protocols
Lina Osama Zaki Quteineh | Consultant Medical Genetics | DHA Registration ID: 9294403
“I understand that undergoing genetic testing for a rare childhood disorder can be emotionally overwhelming. Every result must be interpreted together with clinical findings, enzyme assays, and imaging – a negative NGS panel does not preclude Wolman disease if biochemical suspicion remains high. Our genetic counselling team is available for a dedicated post‑test discussion.”
Advisory Protocol
Pre‑Test Guidance
Patients should discuss the implications of genetic results with a qualified genetic counsellor prior to sampling. Informed consent must be obtained in accordance with Federal Decree-Law No. 4 of 2016 on Medical Liability.
Exclusion Criteria
- Minors require written parental/legal guardian consent as per Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields.
- Sample collection must be performed by a DHA‑licensed phlebotomist; self‑drawn FTA cards are not accepted.
- ER Red Flags: If the patient exhibits acute adrenal crisis (vomiting, dehydration, hypotension, salt‑wasting) or severe hypercholesterolemia with cardiovascular symptoms, seek immediate emergency care before scheduling the test.
- This test is not intended for forensic or non‑medical predictive purposes.
Patient FAQ & Clinical Guidance
1. How accurate is the LIPA gene test for Wolman disease?
Our NGS panel achieves 99.9% diagnostic sensitivity, detecting all known pathogenic LIPA variants with complete exon coverage in 3–4 weeks.
2. What sample is needed and how is the collection done?
A simple blood draw is collected at your home by our ISO‑certified VIP Mobile Phlebotomy team (daily 8 AM – 11 PM). Alternatively, extracted DNA or FTA card drop is accepted via secure courier.
3. Will my insurance cover this Wolman disease genetic test in UAE?
Direct billing verification via WhatsApp confirms your insurance coverage instantly; most UAE providers cover genetic diagnostic tests for metabolic disorders.
4. What is the turnaround time for results?
Results are available within 3–4 weeks from sample receipt at our Dubai Healthcare City laboratory.
UAE Regulatory & Data Privacy Adherence
Data Protection & Clinical Safety Framework
All genetic data processing is conducted in full compliance with 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. Patient consent and medical liability protocols adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability. Our laboratory holds ISO 9001:2015 certification (Cert: INT/EGQ/2509DA/3139).
Clinical & Logistical Metadata
| Test Name | LIPA Gene Sequencing for Wolman Disease (NGS) |
| Price (AED) | 2,800 |
| Turnaround Time | 3 – 4 Weeks |
| Sample Type / Matrix | Peripheral Whole Blood (EDTA) – VIP Mobile Phlebotomy & Cold-Chain Home Collection |
| Methodology Used | Next‑Generation Sequencing (NGS) with bioinformatics confirmation |
| ICD-10-CM Code | E75.5 (Lysosomal acid lipase deficiency) |
| LOINC Code | 75430-1 (LIPA gene mutations detected in Blood or Tissue by Sequencing) |
| DHA Facility License & Address | License No. 1143 – Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians