Test Price
2,800 AED✅ Home Collection Available
TERT Gene Sequencing (NGS) for Pulmonary Fibrosis & Bone Marrow Failure Telomeropathy – 2800 AED – DHA-Approved Genetic Test
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Certified Laboratory (Cert: INT/EGQ/2509DA/3139).
- 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 for result interpretation by medical team.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The TERT Gene Sequencing Test utilizes Next-Generation Sequencing (NGS) to analyze the entire TERT coding region for pathogenic variants associated with familial pulmonary fibrosis and telomere-related bone marrow failure syndromes. This comprehensive genetic screening empowers early risk assessment, precise diagnosis, and tailored clinical surveillance.
Method Comparison
| Feature | Our Test (NGS) | Conventional Sanger Sequencing |
|---|---|---|
| Precision | Full gene coverage, all variant types | Limited to targeted exons, may miss large rearrangements |
| Method | Next-Generation Sequencing (Illumina platform) | Capillary electrophoresis |
| Turnaround Time | 3–4 Weeks | 4–6 Weeks |
Our NGS test delivers superior sensitivity and comprehensive variant detection.
Physician Insight & Safety Protocols
“As a genetic specialist, I emphasize that TERT gene sequencing provides crucial early insights into telomere biology disorders, but it must be interpreted alongside clinical history and family pedigree. Patients should remain under continuous care and never adjust their treatment without medical consultation.”
— Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
🚨 Medication Advisory
Do not discontinue prescribed medication without consulting your doctor. Genetic information is not a substitute for ongoing clinical management.
Exclusion Criteria & Emergency Red Flags
- Exclusion Criteria: Acute febrile illness, hemodynamic instability, inability to provide informed consent, absence of pre-test genetic counseling, or known contraindication to venipuncture.
- Emergency Red Flags: If you experience sudden shortness of breath, chest pain, high fever with bleeding or bruising, or any sign of acute respiratory distress, seek immediate medical attention at the nearest emergency department.
Patient FAQ & Clinical Guidance
1. What conditions does the TERT gene sequencing test detect?
Answer: This test identifies TERT gene mutations linked to pulmonary fibrosis and bone marrow failure syndromes. These include familial idiopathic pulmonary fibrosis, dyskeratosis congenita, and aplastic anemia caused by telomere dysfunction. The result helps doctors assess disease risk and plan surveillance.
2. How long does it take to receive results?
Answer: Results are typically available within 3 to 4 weeks from the date of sample collection. The turnaround time ensures meticulous sequencing, bioinformatics analysis, and expert clinical interpretation. A final report will be shared with your ordering physician.
3. Do I need any special preparation before the test?
Answer: A pre-test genetic counseling session is mandatory to discuss implications and draw a pedigree chart. No fasting is required for blood collection. Please provide a detailed clinical history and any relevant family records to ensure accurate variant interpretation.
UAE Regulatory & Data Privacy Adherence
This genetic test adheres strictly 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. All specimen handling and data processing comply with Federal Decree-Law No. 4 of 2016 on Medical Liability for patient safety and informed consent. Laboratory operations are ISO 9001:2015 certified (Cert: INT/EGQ/2509DA/3139).
Clinical & Logistical Metadata
| Test Name | TERT Gene Sequencing (NGS) for Pulmonary Fibrosis & Bone Marrow Failure Telomeropathy |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3–4 Weeks |
| Sample Type / Matrix | Peripheral Whole Blood (EDTA tube) – VIP Mobile Phlebotomy available |
| Methodology Used | Next-Generation Sequencing (NGS) – Illumina platform, full gene coverage |
| ICD-10-CM Code | J84.112 (Familial pulmonary fibrosis), D61.9 (Aplastic anemia), Z15.89 (Genetic susceptibility) |
| LOINC Code | 82182-7 (TERT gene targeted mutation analysis by Sequencing) |
| 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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