Test Price
2,800 AED✅ Home Collection Available
GTPBP2 Gene Neurodegeneration with Brain Iron Accumulation Genetic Test in UAE | 2800 AED | DHA Licensed
Executive Summary & Core Metrics
Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Next-Generation Sequencing.
- 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 Interpretation Support with a Genetic Counsellor.
- Insurance: Direct Billing Verification via WhatsApp at +971 54 548 8731.
Test Overview & Methodology
The GTPBP2 Genetic Test detects pathogenic variants in the entire coding region of the GTPBP2 gene, enabling precise molecular diagnosis of neurodegeneration with brain iron accumulation (NBIA) in individuals and at-risk family members. It uses Next-Generation Sequencing (NGS) — the gold‑standard technology — to deliver a comprehensive analysis with a rapid turnaround time of 3‑4 weeks at a cost of 2800 AED.
| Feature | Our Test (Premium NGS) | Closest Alternative (Sanger Single‑Gene Sequencing) |
|---|---|---|
| Methodology | Next-Generation Sequencing (NGS) – full gene coverage | Sanger sequencing – selected exons only |
| Diagnostic Sensitivity | 99.9% (includes deep intronic variants) | ~95% (limited to targeted regions) |
| Turnaround Time | 3–4 weeks | 6–8 weeks |
| Clinical Support | Included: telephonic genetic counselling & post-test interpretation | Often not included |
Physician Insight & Safety Protocols
“Genetic testing must always be interpreted within the full clinical picture. A positive GTPBP2 variant can confirm a diagnosis of NBIA and guide family planning, but a negative result does not exclude other genetic or acquired causes of neurodegeneration. Please discuss all results with your neurologist or clinical geneticist.”
— Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
Medication Advisory
Do not discontinue any prescribed medication without first consulting your supervising doctor.
Exclusion Criteria & Emergency Red Flags
- Active severe infection or uncontrolled systemic illness that may compromise sample quality.
- Bleeding disorder or anticoagulant therapy that poses a risk for phlebotomy (alternative oral swab collection may be arranged).
- Acute neurological deterioration (e.g., new‑onset seizures, loss of consciousness, stroke‑like symptoms) — seek emergency medical care immediately.
- Known allergy to materials used in blood collection (e.g., latex, antiseptic).
- Children under 2 years – require a paediatric phlebotomist and additional parental consent per UAE regulations.
Patient FAQ & Clinical Guidance
1. What does the GTPBP2 genetic test actually look for?
Our NGS assay sequences the entire GTPBP2 gene to identify single nucleotide variants, small deletions/duplications, and copy number changes that cause neurodegeneration with brain iron accumulation.
2. How should I prepare for the blood collection?
No fasting or dietary changes are required; simply provide your clinical history and any relevant medical reports before the home phlebotomy visit.
3. When will I receive my results and who will explain them?
Your full report is delivered within 3–4 weeks, and a complimentary telephonic consultation with a genetic counsellor is included to interpret the findings.
UAE Regulatory & Data Privacy Adherence
Regulatory Compliance
All genetic tests adhere to 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 follow Federal Decree-Law No. 4 of 2016 on Medical Liability.
Data Privacy: Patient data is encrypted and stored on UAE-based servers. Report sharing requires explicit informed consent.
DHA/MOHAP Standards: Nomenclature follows DHA Molecular Pathology Guidelines. NGS is the recommended technique.
Clinical & Logistical Metadata
| Test Name | GTPBP2 Gene Sequencing for Neurodegeneration with Brain Iron Accumulation |
| Price (AED) | 2,800 |
| Turnaround Time | 3–4 weeks |
| Sample Type / Matrix | Whole Blood (Peripheral) – VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection |
| Methodology Used | Next-Generation Sequencing (NGS) |
| ICD-10-CM Code | G23.0 (Hallervorden-Spatz disease / NBIA) |
| LOINC Code | 55233-1 (Genetic analysis for specific gene) |
| DHA Facility License & Laboratory Address | DHA Facility License Number: 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