Test Price
4,800 AED✅ Home Collection Available
Neuronal Ceroid Lipofuscinosis Gene Panel in UAE | 4800 AED
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing.
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Daily 8 AM – 11 PM).
- Clinical Guidance: Telephonic Post-Test Guidance from a Consultant Medical Geneticist.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The Neuronal Ceroid Lipofuscinosis (NCL) Gene Panel screens for pathogenic variants in genes associated with a group of inherited neurodegenerative disorders. Using high-depth Next Generation Sequencing, it covers all known NCL loci (CLN1–CLN14, KCTD7, MFSD8, etc.) with bioinformatic confirmation, enabling early diagnosis and family planning.
| Feature | Our NCL Gene Panel | Closest Alternative |
|---|---|---|
| Precision | High-depth NGS covering all known NCL loci (CLN1–CLN14, KCTD7, MFSD8, etc.) | Single-gene testing or WES with limited phenotype-driven interpretation |
| Methodology | Next Generation Sequencing (NGS) with bioinformatic confirmation | Sanger sequencing for individual genes |
| Turnaround Time | 4–6 weeks, including expert clinical correlation | 4–8 weeks for stepwise single-gene approach |
Physician Insight & Safety Protocols
“As a Consultant Medical Geneticist, I emphasize that NCL gene panel results must be interpreted alongside neurological and ophthalmological assessments. The test is highly sensitive but not a substitute for clinical judgment. Always discuss findings with a genetic counselor to understand their full impact.” — Lina Osama Zaki Quteineh, Consultant Medical Genetics (DHA Registration ID: 9294403)
Medication Advisory
Do not discontinue prescribed medication without consulting your doctor. This panel does not replace therapeutic decisions.
Safety & Exclusion Criteria
- Pregnancy or suspected pregnancy: Invasive sample collection (e.g., amniocentesis) requires specialist approval.
- Active infection at collection site; bleeding disorders uncontrolled by medication.
- ER Red Flags: Sudden vision loss, uncontrollable seizures, or acute neurological regression — seek immediate emergency care before genetic testing.
Patient FAQ & Clinical Guidance
1. What does the NCL Gene Panel detect?
Our panel detects pathogenic variants across 14 NCL-related genes with 99.9% sensitivity, enabling early diagnosis even before symptoms appear.
2. How is the sample collected and is it safe for children?
A trained phlebotomist performs a minimally invasive peripheral blood draw under strict aseptic conditions. For prenatal testing, amniotic fluid collection is hospital-only and requires specialist oversight.
3. Will my insurance cover the cost?
Direct billing verification is available via WhatsApp at +971 54 548 8731; many UAE insurers cover NCL panels when medically necessary.
UAE Regulatory & Data Privacy Adherence
This test complies 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. Clinical safety and patient consent adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability. Our facility is ISO 9001:2015 Certified (Cert: INT/EGQ/2509DA/3139).
Clinical & Logistical Metadata
| Test Name | Neuronal Ceroid Lipofuscinosis Gene Panel |
| Price (AED) | 4,800 |
| Turnaround Time | 4–6 weeks |
| Sample Type / Matrix | Whole Blood (Peripheral) |
| Methodology Used | Next Generation Sequencing (NGS) with bioinformatic confirmation |
| ICD-10-CM Code | E75.4, Z13.9 |
| LOINC Code | 96623-4 |
| 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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ISMS 27001:2022
ISO Accredited
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All reports reviewed by DHA-Certified physicians