Test Price
2,800 AEDโ Home Collection Available
CLIC2 Gene X-Linked Intellectual Disability Type 32 Genetic Test (NGS) in UAE | 2,800 AED | DHA Licensed
Executive Summary & Core Metrics
Accuracy Guarantee
99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited NGS 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 for result interpretation with a DHA-licensed Consultant Medical Geneticist.
Insurance
Direct Billing Verification via WhatsApp +971 54 548 8731.
The CLIC2 NGS test delivers definitive molecular confirmation for X-linked intellectual disability type 32, enabling targeted medical management and informed genetic counselling. This accredited diagnostic pathway is fully compliant with UAE federal data protection and healthcare information standards.
Test Overview & Methodology
The CLIC2 NGS test sequences the entire coding region of the chloride intracellular channel 2 gene to identify pathogenic variants responsible for X-linked intellectual disability type 32. This condition primarily affects males, presenting with developmental delay, cognitive impairment, and often behavioural abnormalities; early molecular confirmation enables tailored medical management and genetic counselling.
Next-Generation Sequencing with Sanger confirmation detects single-nucleotide variants and small insertion/deletion events at over 99% clinical sensitivity for pathogenic alterations within CLIC2. The workflow follows ISO 9001:2015 accredited protocols with full DHA oversight.
| Features | Our Test โ CLIC2 NGS | Closest Alternative โ Chromosomal Microarray (CMA) |
|---|---|---|
| Precision | Single-nucleotide variant & small indel detection within CLIC2 | Detects only large deletions/duplications >50 kb; misses point mutations |
| Method | Next-Generation Sequencing (Illumina) with Sanger confirmation | Array-based comparative genomic hybridisation (aCGH) |
| Turnaround Time | 3 to 4 weeks | 2 to 4 weeks |
| Clinical Sensitivity for CLIC2 | >99% for pathogenic variants in the target gene | Near 0% for intragenic mutations; not designed for single-gene disorders |
Physician Insight & Safety Protocols
โA CLIC2 pathogenic result carries pivotal implications for developmental prognosis, recurrence risk estimation, and cascade testing of at-risk female carriers. This molecular assay must be integrated with a complete clinical assessment and neurodevelopmental evaluation. A normal result does not exclude alternative genetic or acquired aetiologies of intellectual disability. Mandatory post-test genetic counselling is required to contextualise findings and guide long-term management.โ
โ Lina Osama Zaki Quteineh, Consultant Medical Genetics & DHA-Registered Specialist (DHA: 9294403)
Medication Advisory
โ Medication Advisory
Do not discontinue prescribed medication or modify any therapy without consulting your treating physician. This genetic test is for diagnostic and counselling purposes only; it does not replace ongoing clinical management.
Safety Exclusion Criteria & Emergency Red Flags
Exclusion Criteria & Precautions
- Exclusion: Active infection or fever (>38ยฐC) at time of blood draw; history of heparin-induced thrombocytopenia (for FTA card method).
- Exclusion: Patient unable to provide voluntary informed consent, or legal guardian consent for minors as per Federal Decree-Law No. 4 of 2016 on Medical Liability and applicable UAE genetic testing regulations.
- Emergency Red Flags: If the patient experiences acute neurological decompensation (new-onset seizures, loss of consciousness, or stroke-like symptoms), seek immediate medical attention โ do not wait for genetic results.
- Emergency Red Flags: Any unexplained bleeding or severe hematoma after sample collection requires urgent medical review.
Patient FAQ & Clinical Guidance
1. What is the CLIC2 gene test, and why is it performed?
The CLIC2 NGS test analyzes the entire coding region of the CLIC2 gene to detect pathogenic variants causing X-linked intellectual disability type 32, aiding accurate diagnosis and informed family counselling.
2. How long do results take, and what sample is required?
A standard peripheral whole blood sample or one drop of blood on an FTA card is required; results are reported within 3 to 4 weeks via DHA-accredited laboratory protocols.
3. What should I expect during the home collection visit?
A DHA-licensed phlebotomist arrives with a temperature-controlled transport kit, performs a quick venipuncture, and completes the cold-chain logistics within 45 minutes.
UAE Regulatory & Data Privacy Adherence
UAE Legal & Data Privacy Compliance: This genetic test is performed in strict accordance 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. All patient genomic data is encrypted, processed exclusively within the UAE, and subject to mandatory informed consent protocols. Our facilities hold ISO 9001:2015 certification (Cert: INT/EGQ/2509DA/3139) and are licensed by Dubai Health Authority (Facility License 1143).
Clinical & Logistical Metadata
| Test Name | CLIC2 Gene X-Linked Intellectual Disability Type 32 Genetic Test (NGS) |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3 to 4 weeks |
| Sample Type / Matrix | Peripheral Whole Blood or Dried Blood Spot (FTA Card) |
| Methodology Used | Next-Generation Sequencing (NGS) with Sanger Confirmation |
| ICD-10-CM Code | F78 (Other genetic intellectual disabilities) |
| LOINC Code | 51966-0 (DNA sequencing) |
| DHA Facility License & Address | DHA License: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE โ DNA Labs UAE |
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All reports reviewed by DHA-Certified physicians