Test Price
2,800 AED✅ Home Collection Available
SLC2A1 Gene Paroxysmal Exercise-Induced Dyskinesia with Epilepsy and/or Hemolytic Anemia Genetic Test in UAE
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing, using clinically validated NGS (Next‑Generation Sequencing) technology.
- 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 in result interpretation by a DHA-licensed Consultant Medical Geneticist.
- Insurance: Direct Billing Verification via WhatsApp at +971 54 548 8731.
- Price: 2,800 AED — includes full gene sequencing, MLPA for CNVs, and a comprehensive clinical report.
Test Overview & Methodology
This advanced NGS-based genetic test analyzes the entire SLC2A1 gene for pathogenic variants associated with glucose transporter type 1 deficiency syndrome (GLUT1-DS), which presents with paroxysmal exercise-induced dyskinesia, epilepsy, and/or hemolytic anemia. The test enables definitive molecular diagnosis, guiding targeted dietary therapy (ketogenic diet) and antiepileptic management. Full gene coverage includes deep intronic regions and copy-number variant detection via MLPA.
| Parameter | Our Test (SLC2A1 NGS) | Closest Alternative (Single‑Gene Sequencing) |
|---|---|---|
| Precision | >99.9% analytical sensitivity, full gene coverage including deep intronic regions | ~98% for exonic SNVs; may miss copy‑number variants |
| Method | Next‑Generation Sequencing (NGS) with MLPA backup for CNVs | Sanger sequencing of selected exons only |
| Turnaround | 3–4 weeks (expedited reporting available) | 4–6 weeks |
Physician Insight & Safety Protocols
"A positive SLC2A1 genetic test provides a definitive molecular confirmation of GLUT1 deficiency syndrome, which is critical for initiating early ketogenic dietary therapy and avoiding unnecessary antiepileptic trials. However, a negative result does not exclude the clinical diagnosis; phenotype-driven metabolic assessments and a trial of ketogenic diet remain essential. Close multidisciplinary collaboration between neurologists, haematologists, and clinical geneticists is the cornerstone of optimal patient outcomes."
— Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
Advisory — Medication Continuation
Do not discontinue prescribed antiepileptic drugs or other medications without consulting your doctor. Abrupt withdrawal may provoke severe seizure exacerbation or status epilepticus. Continue all current therapies until your genetic results are reviewed by your treating physician.
Exclusion Criteria & Clinical Red Flags
- Exclusion Criteria: Unstable cardiorespiratory status, acute febrile illness within 48 hours of sample collection, known hypersensitivity to phlebotomy materials.
- Emergency Red Flags (seek immediate medical attention, not this test): Loss of consciousness with prolonged convulsions, difficulty breathing, sudden onset of severe headache with altered sensorium, or haemoglobin drop below 7 g/dL with haemodynamic instability.
Patient FAQ & Clinical Guidance
1. What symptoms or conditions would prompt this SLC2A1 gene test?
A neurologist or geneticist recommends this test when a child or adult presents with paroxysmal movement problems triggered by exercise, combined with epilepsy, developmental delay, or unexplained haemolytic anaemia. Early genetic diagnosis enables targeted dietary intervention with a ketogenic diet and appropriate seizure management.
2. How do I prepare for the blood collection, and can it be done at home?
No fasting is required; simply ensure the skin is clean and free of lotions. Our DHA-certified mobile phlebotomy team collects the sample at your home between 8 AM and 11 PM daily, maintaining cold-chain integrity throughout transport to the laboratory.
3. What happens after a positive or negative result?
A positive result confirms GLUT1 deficiency syndrome and opens access to ketogenic diet therapy and specific seizure medications. A negative result does not entirely rule out the condition; your specialist may recommend additional metabolic testing, functional studies, or periodic re-evaluation based on your clinical presentation.
4. How long does it take to receive results, and how will they be delivered?
The standard turnaround time is 3–4 weeks from sample receipt. Results are delivered via a secure digital portal and a printed clinical report. A DHA-licensed genetic counsellor provides a telephonic explanation of the findings and coordinates follow-up care as needed.
UAE Regulatory & Data Privacy Adherence
All genetic testing services at DNA Labs UAE are conducted in full compliance with:
- Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) — governing the lawful collection, processing, and storage of personal and genetic data.
- Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields — regulating health information systems and digital health data security.
- Federal Decree-Law No. 4 of 2016 on Medical Liability — ensuring clinical safety and informed patient consent throughout the testing pathway.
- ISO 9001:2015 — certified quality management system (Cert: INT/EGQ/2509DA/3139).
All samples are processed in our DHA-licensed facility. Your genetic data remains confidential and is never shared with third parties without your explicit written consent.
Clinical & Logistical Metadata
| Test Name | SLC2A1 Gene Paroxysmal Exercise-Induced Dyskinesia with Epilepsy and/or Hemolytic Anemia Genetic Test |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3–4 Weeks (expedited reporting available) |
| Sample Type / Matrix | Peripheral Whole Blood |
| Methodology Used | Next-Generation Sequencing (NGS) with MLPA Backup for CNVs |
| ICD-10-CM Code | E74.8 |
| LOINC Code | 21641-9 |
| DHA Facility License & Laboratory Address | DHA License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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