Test Price
2,800 AED✅ Home Collection Available
SLC25A22 Gene Early Infantile Epileptic Encephalopathy Type 3 Genetic Test in UAE | 2800 AED | DHA Licensed
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 15189 Accredited Genetic Testing.
- 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 Correlation and Result Interpretation included.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The SLC25A22 gene test uses Next Generation Sequencing (NGS) to detect pathogenic variants causing Early Infantile Epileptic Encephalopathy Type 3 (EIEE3), a severe neonatal-onset epilepsy. Full gene sequencing with orthogonal Sanger confirmation ensures highest diagnostic yield.
| Parameter | Our Test (Premium NGS) | Closest Alternative (Broad Panel/WES) |
|---|---|---|
| Precision | Full gene sequencing with Sanger confirmation; variant-level resolution | Wider coverage but may miss deep intronic or regulatory variants |
| Method | NGS + orthogonal validation; 100-bp paired-end reads | Varies – often only NGS without dedicated confirmation |
| Turnaround Time | 3–4 weeks | 6–8 weeks (typical for exomes) |
Physician Insight & Safety Protocols
“As a Consultant Medical Genetics, I emphasize that a positive SLC25A22 result confirms the genetic aetiology and enables precise prognosis. Clinical correlation with EEG and seizure semiology remains essential for comprehensive care.”
— Lina Osama Zaki Quteineh | Consultant Medical Genetics | DHA Registration ID: 9294403
⚠ Medication Advisory
Do not discontinue or adjust any anti‑epileptic medication without consulting your treating physician.
Safety Exclusion Criteria & ER Red Flags
- Do not book if: patient is haemodynamically unstable, febrile, or requires emergency intervention.
- ER red flags: new‑onset status epilepticus, respiratory distress, or signs of increased intracranial pressure.
Patient FAQ & Clinical Guidance
1. What does the SLC25A22 NGS test detect and why is it critical for my infant?
It detects pathogenic variants in the SLC25A22 gene that cause early‑infantile epileptic encephalopathy type 3, enabling precise diagnosis, prognosis, and personalized anti‑seizure therapy.
2. How is the sample collected and what pre‑test steps are mandatory?
A single blood draw is collected at home via VIP mobile phlebotomy; mandatory pre‑test genetic counselling and a family pedigree chart are required.
3. Is this covered by UAE insurance and how quickly will I receive the result?
Many UAE insurers cover genetic testing for epileptic encephalopathies with prior approval; results are typically ready in 3–4 weeks. Verify your coverage via WhatsApp.
UAE Regulatory & Data Privacy Adherence
All genetic data is handled in 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. Clinical safety and patient consent align with Federal Decree-Law No. 4 of 2016 on Medical Liability.
Clinical & Logistical Metadata
| Test Name | SLC25A22 Gene Early Infantile Epileptic Encephalopathy Type 3 Genetic Test |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3–4 weeks |
| Sample Type / Matrix | Peripheral whole blood (3–5 mL in EDTA tube); VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection |
| Methodology Used | Next Generation Sequencing (NGS) with Sanger confirmation; 100-bp paired-end reads |
| ICD-10-CM Code | G40.5 (Epileptic encephalopathy) |
| LOINC Code | 21656-5 (Gene mutations detected by sequencing) |
| 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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