Test Price
3,000 AED✅ Home Collection Available
Lysosomal Storage Disorders (LSD) Enzyme Panel Genetic Test in UAE | 3000 AED | Next-Generation Sequencing
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% diagnostic sensitivity for target variants 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 by DHA-licensed physicians for result interpretation and genetic counseling referral.
- Insurance: Direct billing verification via WhatsApp at +971 54 548 8731.
Test Overview & Methodology
This next-generation sequencing (NGS) panel analyzes a comprehensive set of genes associated with lysosomal storage disorders (LSDs), providing detailed enzyme deficiency insights in a single streamlined workflow. The test detects pathogenic single-nucleotide variants, insertions, deletions, and copy number variations across all targeted genes, enabling early diagnosis, carrier screening, and informed genetic counseling.
| Feature | Our NGS Panel | Closest Alternative (Biochemical Enzyme Assays) |
|---|---|---|
| Diagnostic Sensitivity | >99.9% for target variants | ~85–90% (limited by enzyme expression) |
| Methodology | NGS (Next Generation Sequencing) with CNV analysis | Fluorometric / spectrophotometric enzyme activity |
| Turnaround Time | 3 to 4 Weeks | 1–2 Weeks (limited scope) |
| Genes Covered | Comprehensive panel (GBA, GLA, SMPD1, GAA, IDUA, GALC, and others) | Single‑enzyme testing per assay |
Physician Insight & Safety Protocols
"As a Consultant in Medical Genetics, I want to emphasize that this NGS panel is a powerful diagnostic aid for lysosomal storage disorders. However, results must always be interpreted in the full context of the patient's clinical presentation, family pedigree, and prior biochemical findings. I strongly encourage all patients and families to participate in post-test genetic counseling to fully understand variant implications and recurrence risks."
– Ms. Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
Important Medical Advisory
Never discontinue, adjust, or initiate prescribed medications based solely on genetic test results without consulting your treating physician. Medication management requires clinical correlation and professional oversight.
Exclusion Criteria & Emergency Red Flags
- Test Exclusion: This panel is not intended for acute crisis diagnosis. If the patient is experiencing severe metabolic decompensation (e.g., rapid neurological deterioration, acute organ failure, respiratory distress), seek emergency medical care immediately.
- Emergency Red Flags: Unexplained severe bone pain, sudden vision or hearing loss, progressive muscle weakness, severe abdominal distension, or altered mental status require immediate hospital evaluation.
- Minor Consent: In accordance with Federal Decree-Law No. 4 of 2016 on Medical Liability and UAE federal regulations governing genetic testing, testing on minors requires informed parental or guardian consent along with a pre-test genetic counseling session.
Patient FAQ & Clinical Guidance
1. What is the Lysosomal Storage Disorders Enzyme Panel Genetic Test?
This test uses next-generation sequencing (NGS) to analyze multiple genes associated with lysosomal storage diseases, detecting pathogenic variants that cause enzyme deficiencies. It enables early diagnosis, carrier screening, and informed family planning decisions.
2. How should I prepare for this test?
Preparation involves a thorough clinical history review and a pre-test genetic counseling session to document a detailed pedigree chart, especially when multiple family members are affected. No special dietary or medication restrictions are typically required unless specified by your physician.
3. How long does it take to receive results?
The turnaround time is 3 to 4 weeks from sample receipt at our ISO-certified laboratory. Complex cases with multiple variants or requiring orthogonal confirmation may need additional interpretation time.
4. What kind of sample is required for this test?
This test requires a standard peripheral whole blood sample collected in an EDTA tube. Our VIP Mobile Phlebotomy service can collect the sample at your home between 8 AM and 11 PM daily via temperature-controlled cold-chain logistics.
5. Will my insurance cover this genetic test?
Coverage depends on your individual insurance policy and pre-authorization requirements. You can verify direct billing options by contacting us via WhatsApp at +971 54 548 8731 with your insurance details.
UAE Regulatory & Data Privacy Adherence
Your data privacy and safety are protected under UAE federal law. DNA Labs UAE operates in full compliance with:
- Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) – governing the collection, processing, and storage of personal health data.
- Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields – regulating digital health records and telemedicine frameworks.
- Federal Decree-Law No. 4 of 2016 on Medical Liability – ensuring clinical safety, informed consent, and medical professional accountability.
All genetic data is encrypted, access-controlled, and retained only for the validated clinical purpose. Our laboratory is ISO 9001:2015 certified (Cert: INT/EGQ/2509DA/3139) and fully licensed by the Dubai Health Authority.
Clinical & Logistical Metadata
| Test Name | Lysosomal Storage Disorders (LSD) Enzyme Panel Genetic Test (NGS) |
| Price (AED) | 3,000 AED |
| Turnaround Time | 3 to 4 Weeks |
| Sample Type / Matrix | Whole Blood (Peripheral) – EDTA tube |
| Methodology Used | Next Generation Sequencing (NGS) with CNV analysis |
| ICD-10-CM Code | E75.2, E75.6 |
| LOINC Code | 81247-9 |
| DHA Facility License & Laboratory Address | License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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