Test Price
2,800 AED✅ Home Collection Available
CSTB Gene (Unverricht-Lundborg Disease) Genetic Test in UAE | 2800 AED
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited NGS Processing.
- 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 for result interpretation.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
Unverricht-Lundborg disease (EPM1) is a rare, progressive myoclonic epilepsy caused by mutations in the CSTB gene. This genetic test is processed at a DHA-licensed molecular genetics facility using next-generation sequencing (NGS) for comprehensive variant detection, with a typical turnaround of 3–4 weeks.
| Feature | Our Test (CSTB NGS) | Closest Alternative (Sanger Sequencing) |
|---|---|---|
| Method | Next-Generation Sequencing (NGS) | Sanger sequencing (single‑gene) |
| Variant Detection | Full gene – SNVs, indels, CNV screening | Point mutations and small deletions only |
| Turnaround Time | 3–4 weeks | 4–6 weeks |
| Diagnostic Yield | >98% for CSTB mutations | ~90% |
| Price (AED) | 2800 | 2500 – 3000 (varies) |
| DHA/MOHAP Standard | Fully compliant (NGS panel) | Legacy method, not optimized for NGS |
Physician Insight & Safety Protocols
“As a consultant medical geneticist, I emphasize that the CSTB gene test provides a definitive molecular diagnosis for Unverricht-Lundborg disease. However, genetic results must be interpreted alongside clinical phenotype, EEG findings, and family history. Pre‑ and post‑test genetic counseling is essential for families to understand the implications and management.”
— Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA License 9294403
⚠ Medication Warning
Do not discontinue prescribed antiepileptic medication without consulting your doctor. Abrupt withdrawal can provoke life‑threatening seizures.
Exclusion Criteria & Emergency Red Flags
- Recent blood transfusion (within 12 weeks) – may interfere with DNA-based testing.
- Lack of informed consent and pre‑test genetic counseling for minors (mandatory per Federal Decree-Law No. 4 of 2016 on Medical Liability).
- Patient/family unable to provide a four‑generation pedigree required for accurate interpretation.
- Emergency red flags: New prolonged seizure (>5 min), status epilepticus, sudden deterioration in gait or cognition – seek immediate emergency care, do not wait for genetic results.
Patient FAQ & Clinical Guidance
1. What does the CSTB gene test detect?
This NGS test detects disease‑causing mutations in the CSTB gene responsible for Unverricht‑Lundborg disease, enabling early and accurate diagnosis.
2. Is a doctor’s referral required, and can children be tested?
Yes, a referral from a neurologist or clinical geneticist is mandatory. For minors, written parental consent and a genetic counseling session are compulsory under UAE Federal Decree-Law No. 4 of 2016 on Medical Liability.
3. How long does the result take, and what happens after?
Results are typically ready in 3–4 weeks. Afterward, you receive a telephonic clinical guidance session to explain the genetic report and recommend next steps.
UAE Regulatory & Data Privacy Adherence
This genetic testing service fully complies with Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) for genetic data privacy, as well as Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. Clinical safety and patient consent are governed by Federal Decree-Law No. 4 of 2016 on Medical Liability. The laboratory operates under DHA Facility License 1143 and is ISO 9001:2015 certified (Cert: INT/EGQ/2509DA/3139).
Clinical & Logistical Metadata
| Test Name | CSTB Gene (Unverricht-Lundborg Disease) Genetic Test |
| Price (AED) | 2800 |
| Turnaround Time | 3–4 weeks |
| Sample Type / Matrix | Peripheral whole blood (EDTA) |
| Methodology Used | Next-Generation Sequencing (NGS) |
| ICD-10-CM Code | G40.3 |
| LOINC Code | 21665-4 |
| DHA Facility License & Address | License 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