Test Price
2,800 AEDโ Home Collection Available
AP1S2 Gene X-Linked Intellectual Disability (XLID) Type 59 Genetic Test โ Dubai, UAE
Executive Summary & Core Metrics
Executive Summary โ Your Clinical Peace of Mind
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 accredited NGS processing.
- Premium Phlebotomy Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Available daily from 8 AM to 11 PM).
- Clinical Guidance: Telephonic Post-Test Genetic Counselling with a Consultant Medical Geneticist.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
The AP1S2 genetic test is a definitive molecular diagnostic tool for X-linked intellectual disability type 59. Our fully accredited Next-Generation Sequencing (NGS) approach provides rapid, high-confidence results, supported by professional genetic counselling and a dedicated clinical team.
Test Overview & Methodology
The AP1S2 gene test diagnoses X-linked intellectual disability type 59, a rare neurodevelopmental disorder primarily affecting males, by sequencing the entire coding region via Next-Generation Sequencing. Early diagnosis enables precise genetic counselling, targeted management, and family planning. Our methodology uses high-depth NGS to detect single nucleotide variants, small insertions/deletions, and copy number variants within the AP1S2 gene.
| Feature | Our AP1S2 XLID NGS Test | Closest Alternative |
|---|---|---|
| Gene Coverage | Full AP1S2 gene โ all exons and splice sites | Targeted analysis for known familial variant only |
| Methodology | NGS (High-Depth Sequencing) | Sanger sequencing |
| Diagnostic Sensitivity | 99.9% | ~95% (mutation known) |
| Turnaround Time | 3โ4 Weeks | 4โ6 Weeks |
| Price (AED) | 2800 | ~1500 (limited scope) |
| Accreditation | ISO 9001:2015 & DHA Licensed | Variable |
Physician Insight & Safety Protocols
"Having walked alongside families affected by neurodevelopmental conditions, I know that a definitive genetic answer can offer direction and hope. The AP1S2 test is a robust tool, but its results must always be woven into the full clinical picture and discussed with a specialistโnever used in isolation. My team and I are committed to guiding you through every step, from pre-test counseling to post-result care planning."
โ Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
Clinical Advisory
Patient Safety โ Exclusion Criteria & Emergency Red Flags
Exclusion Criteria (Please Inform Our Team Before Scheduling):
- Active severe infection or febrile illness requiring urgent medical attention.
- Inability to provide informed consent or lack of a legal guardian for minors (consistent with Federal Decree-Law No. 4 of 2016 on Medical Liability).
- Unstable psychiatric condition that could compromise safe sample collection.
ER Red Flags โ Seek Immediate Medical Care If:
- Sudden severe headache, visual changes, or loss of consciousness.
- New-onset seizures or prolonged convulsions.
- Acute behavioural regression, confusion, or unresponsiveness.
Sample Collection Protocol
This test requires a standard peripheral whole blood sample. Our logistics team provides VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection, available daily from 8 AM to 11 PM. Pre-test genetic counselling is mandatory to ensure informed consent and to gather a detailed family pedigree.
Patient FAQ & Clinical Guidance
1. What does the AP1S2 gene test for XLID type 59 detect?
The AP1S2 Genetic Test detects pathogenic DNA variants in the AP1S2 gene responsible for X-linked intellectual disability type 59. This test sequences all coding regions with high depth, identifying single nucleotide changes, small insertions/deletions, and copy number variants that impair protein function and lead to neurodevelopmental delay. Genetic counselling is provided before and after testing to interpret the findings appropriately.
2. How is the sample collected and what are the pre-test requirements?
A blood sample is collected via our VIP Mobile Phlebotomy service by DHA-licensed nurses. You must attend a mandatory pre-test genetic counselling session to draw a detailed pedigree chart of affected family members. Fasting is not required, and our team handles all cold-chain logistics for sample integrity under ISO 9001:2015 standards.
3. What is the turnaround time and how will I receive results?
Results are delivered securely within 3-4 weeks via an encrypted online portal with a telephonic counselling session from our genetics team. You will receive a comprehensive report, including variant classification and clinical interpretation, followed by a private consultation with our Consultant Medical Geneticist to discuss next steps and family implications, all compliant with UAE PDPL data privacy laws.
UAE Regulatory & Data Privacy Adherence
Accreditation & Legal Compliance: DNA Labs UAE operates under ISO 9001:2015 certification and is fully licensed by the Dubai Health Authority (DHA). We adhere strictly to Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) for all patient data handling and privacy protocols. Our clinical safety and patient consent procedures comply with Federal Decree-Law No. 4 of 2016 on Medical Liability. Additionally, our health information technology systems are compliant with Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields.
Clinical & Logistical Metadata
| Test Name | AP1S2 Gene X-Linked Intellectual Disability (XLID) Type 59 Genetic Test |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3โ4 Weeks |
| Sample Type / Matrix | Peripheral Whole Blood (3โ5 mL in EDTA tube) |
| Methodology Used | Next-Generation Sequencing (NGS) โ High-Depth Whole Gene Sequencing |
| ICD-10-CM Code | F70, Q87.8 |
| LOINC Code | 92878-5 |
| DHA Facility License & Laboratory Address | License No: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | Corporate Lab: DNA Labs UAE |
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Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians