Test Price
2,800 AED✅ Home Collection Available
AGTR2 Gene Intellectual Disability (X-linked, MRX88) Genetic Test in UAE | 2800 AED
Executive Summary & Core Metrics
At DNA Labs UAE, our AGTR2 NGS panel delivers a molecular diagnosis for X‑linked intellectual disability (MRX88) with 99.9% diagnostic sensitivity. We combine ISO‑accredited sequencing, VIP home phlebotomy, and DHA‑licensed clinical interpretation to transform uncertainty into actionable care.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited NGS Processing.
- Premium Logistics: VIP Mobile Phlebotomy & Temperature‑Controlled Cold‑Chain Home Collection (daily 8 AM – 11 PM).
- Clinical Guidance: Telephonic Post‑Test Clinical Interpretation by a DHA‑licensed physician.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The AGTR2 gene provides instructions for a receptor that plays a role in brain development and function. Pathogenic variants in this gene cause an X‑linked form of intellectual disability (MRX88). Our next‑generation sequencing (NGS) panel analyses the full coding region and splice sites of AGTR2, detecting single‑nucleotide variants, small insertions/deletions, and splice‑site mutations with high accuracy. This test is indicated for individuals with unexplained developmental delay, particularly when family history suggests X‑linked inheritance.
| Feature | Our AGTR2 NGS Test | Closest Alternative (Chromosomal Microarray) |
|---|---|---|
| Methodology | Next Generation Sequencing (NGS) – full gene analysis | Chromosomal Microarray (CNV detection) |
| Target Resolution | Single‑nucleotide variants, indels, splice‑site mutations | Large deletions/duplications >50 kb |
| Turnaround Time | 3 – 4 Weeks | 6 – 8 Weeks |
| Diagnostic Yield for ID | High (gene‑specific) | Variable (10–15% in isolated ID) |
| Insurance Direct Billing | ✔ Verified via WhatsApp | Often outpatient only |
Physician Insight & Safety Protocols
“Every family deserves a clear path forward. A positive AGTR2 result is not merely a lab finding; it is the cornerstone for personalised intervention plans, reproductive counselling, and access to targeted therapies. I guide my patients through each step, integrating the genetic information with developmental and neurological assessments to ensure holistic care.”
— Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
⚠ Important Clinical Safety Notice
Do not discontinue any prescribed medication or therapy without consulting your treating physician. This genetic test does not replace ongoing pharmacological management; abrupt cessation of anti‑epileptics, hormonal therapies, or psychotropic drugs may cause serious harm.
Exclusion Criteria & Emergency Red Flags
- Exclusion Criteria: Known severe coagulopathy or active haemorrhage; inability to provide a peripheral venous blood sample; patient must be haemodynamically stable for home collection.
- ER Red Flags Post‑Draw: Sudden severe pain, expanding haematoma, active bleeding despite pressure, or any sign of acute neurological change (e.g., seizure, confusion, loss of consciousness) – seek emergency care immediately.
Patient FAQ & Clinical Guidance
1. What is the AGTR2 gene intellectual disability test?
This advanced NGS test sequences the entire AGTR2 gene to identify mutations responsible for X‑linked intellectual disability, providing a molecular diagnosis. It is indicated for children or adults presenting with unexplained developmental delay, especially when a family history suggests an X‑linked pattern of inheritance. A genetic counseling session is mandatory before sample collection.
2. How is the sample collected and how long do results take?
A certified phlebotomist performs a painless venous blood draw at your home under strict cold‑chain protocols, with results delivered in 3 to 4 weeks. Our team will schedule a convenient home visit (8 AM – 11 PM). The sample is then processed in our ISO 9001:2015‑accredited laboratory using NGS technology, and a telephonic clinical interpretation session is included once results are available.
3. Will my insurance cover this?
We offer direct billing verification via WhatsApp; simply send your insurance card photo to +971 54 548 8731 for immediate eligibility confirmation. Most UAE‑based comprehensive policies, including those from Daman, AXA, and Neuron, cover medically necessary genetic testing when referred by a neurologist or clinical geneticist. Our team will handle all paperwork and pre‑authorization on your behalf.
UAE Regulatory & Data Privacy Adherence
Your Trust Is Protected
DNA Labs UAE strictly adheres to the 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 genetic data is encrypted, access‑controlled, and used solely for diagnostic purposes. Clinical safety and patient consent are governed by Federal Decree-Law No. 4 of 2016 on Medical Liability. You retain full rights to your health information as outlined under UAE law.
Clinical & Logistical Metadata
| Test Name | AGTR2 Gene Intellectual Disability (X-linked, MRX88) Genetic Test |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3 – 4 Weeks |
| Sample Type / Matrix | Peripheral Whole Blood – EDTA (2 mL) – VIP Mobile Phlebotomy |
| Methodology Used | Next Generation Sequencing (NGS) – Full Gene Analysis |
| ICD-10-CM Code | F78 (Other intellectual disabilities) |
| LOINC Code | 82203-0 (Genetic testing for inherited condition) |
| DHA Facility License & Laboratory Address | License #1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE – DNA Labs UAE |
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All reports reviewed by DHA-Certified physicians