Test Price
2,800 AED✅ Home Collection Available
AP1S2 Gene X-Linked Intellectual Disability (XLID) Type 59 Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل الجين AP1S2 للعجز الذهني المرتبط بالصبغي X من النوع 59 في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary – Your Clinical Peace of Mind
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 accredited NGS processing.
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection and VIP Mobile Phlebotomy.
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation with a genetic counsellor.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
يضمن هذا التحليل دقة تشخيصية عالية تصل إلى 99.9% عبر مختبراتنا الحاصلة على شهادة ISO 9001:2015 وخدمة سحب دم منزلي متميزة.
Test Overview & Clinical Utility
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.
يُشخص هذا الاختبار العجز الذهني المرتبط بالصبغي X من النوع 59، وهو اضطراب نادر في النمو العصبي يصيب الذكور بشكل رئيسي، من خلال تسلسل كامل المنطقة المُشفِّرة للجين بتقنية الجيل التالي.
| Feature | Our AP1S2 XLID NGS Test | Closest Alternative |
|---|---|---|
| Gene Coverage | Full AP1S2 gene – 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 | 3–4 Weeks | 4–6 Weeks |
| Price (AED) | 2800 | ~1500 (limited scope) |
| Accreditation | ISO 9001:2015 & DHA Licensed | Variable |
Expert Physician Insight & Safety Protocol
"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 specialist—never used in isolation. My team and I are committed to guiding you through every step, from pre-test counseling to post-result care planning."
— Dr. PRABHAKAR REDDY, DHA License: 61713011, Senior Neurologist & Clinical Geneticist
Patient Safety – 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 (compliance with UAE CDS Law 2026 for minors).
- Unstable psychiatric condition that could compromise safe sample collection.
ER Red Flags – 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.
Frequently Asked Questions (FAQ)
Q1: 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.
يكشف هذا الاختبار الجيني بتقنية NGS عن الطفرات المُمْرِضة في الجين AP1S2 المسببة للعجز الذهني المرتبط بالصبغي X من النوع 59.
Q2: How is the sample collected and what are the pre-test requirements?
A blood sample, FTA card, or extracted DNA is collected via a painless home phlebotomy service by our DHA-licensed nurses. You must attend a mandatory pre- 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.
يتم جمع عينة الدم أو بطاقة FTA أو الحمض النووي المستخلص عبر خدمة سحب الدم المنزلي على يد ممرضين مرخصين من هيئة الصحة بدبي، بعد جلسة استشارة وراثية إلزامية.
Q3: 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 neurologist to discuss next steps and family implications, all compliant with UAE PDPL data privacy laws.
تُسلم النتائج خلال 3-4 أسابيع عبر بوابة إلكترونية آمنة مع جلسة استشارة هاتفية من فريقنا الوراثي، مع الالتزام بقانون حماية البيانات الشخصية الإماراتي.
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توقف عن التخمين. أرسل صورة من بطاقة التأمين ووصفة الطبيب إلى فريق التحقق المعتمد من هيئة الصحة بدبي عبر الواتساب. احصل على تحديث الحالة في دقائق.
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