Test Price
2,800 AED✅ Home Collection Available
GPSM2 Gene (Chudley-McCullough Syndrome) Genetic Test in UAE – 2800 AED
Executive Summary & Core Metrics
Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO‑Accredited NGS Processing.
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 by a certified genetic counselor.
Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
| Parameter | Our Test (DHA‑Listed) | Closest Alternative |
|---|---|---|
| Precision | 99.9% Diagnostic Sensitivity (Full‑gene NGS coverage) | Sanger sequencing (limited exon coverage, lower sensitivity) |
| Method | Next‑Generation Sequencing (NGS) – ISO‑validated | Capillary electrophoresis‑based single‑gene analysis |
| Turnaround Time | 3 to 4 Weeks | 4 to 6 Weeks |
Physician Insight & Safety Protocols
“As a consultant in medical genetics, I recognize the emotional weight a genetic diagnosis carries for families. While this NGS test delivers precise molecular data, the results must always be integrated with a comprehensive clinical assessment and genetic counseling. Please never adjust your child’s treatment plan without consulting your pediatrician or clinical geneticist.”
— Lina Osama Zaki Quteineh (DHA: 9294403), Consultant Medical Genetics
Advisory & Safety Information
Medication Continuation Advisory
Never discontinue prescribed medications without first consulting your attending physician.
Exclusion Criteria & Emergency Red Flags
- No age restrictions for pediatric testing; no specific contraindications. Patients on anticoagulation therapy must follow special phlebotomy instructions provided by the nurse.
- Seek Emergency Care Immediately if: Your child shows acute neurological decline, new‑onset seizures, or signs of elevated intracranial pressure (persistent vomiting, worsening lethargy). Do not await test results before seeking help.
Patient FAQ & Clinical Guidance
1. What is the GPSM2 gene test and why is it needed?
Answer: This NGS‑based test analyzes the GPSM2 gene to diagnose Chudley‑McCullough syndrome, enabling early intervention for sensorineural hearing loss and developmental support.
2. How should I prepare my child for the blood draw?
Answer: No fasting is required. A genetic counseling session and pedigree documentation are mandatory before sample collection to ensure accurate interpretation and comprehensive family history assessment.
3. When will I receive the results and who interprets them?
Answer: Results are delivered within 3–4 weeks. A telephonic post‑test guidance session with a DHA‑licensed clinical geneticist will explain the findings and their implications.
UAE Regulatory & Data Privacy Adherence
✅ ISO 9001:2015 Certified Facility (Cert: INT/EGQ/2509DA/3139) | DHA License No. 1143 | Fully compliant 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. Clinical safety and patient consent governed under Federal Decree-Law No. 4 of 2016 on Medical Liability.
Clinical & Logistical Metadata
| Test Name | GPSM2 Gene (Chudley-McCullough Syndrome) Genetic Test |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3 to 4 Weeks |
| Sample Type / Matrix | Peripheral Whole Blood – VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Available daily from 8 AM to 11 PM) |
| Methodology Used | Next-Generation Sequencing (NGS) – Full Gene Coverage, ISO 9001:2015 Validated |
| ICD-10-CM Code | Q87.8 |
| LOINC Code | 55233-1 |
| DHA Facility License & Laboratory Address | License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE – DNA Labs UAE |
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