Test Price
2,800 AED✅ Home Collection Available
TPM1 Gene Cardiomyopathy, Dilated Type 1Y Genetic Test in UAE | 2800 AED | DHA Guidelines
Executive Summary & Core Metrics
Accuracy Guarantee
ISO 9001:2015 accredited NGS process with 99.9% diagnostic sensitivity for TPM1 variant detection.
Premium Logistics
VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection available daily from 8 AM to 11 PM.
Post-Test Clinical Guidance
Telephonic interpretation of results with a genetic counsellor included in the 2800 AED fee.
Insurance & Billing
Direct insurance verification via WhatsApp: +971 54 548 8731.
Test Overview & Methodology
The TPM1 genetic test uses next-generation sequencing to analyse the entire coding region of the TPM1 gene for pathogenic mutations that cause dilated cardiomyopathy type 1Y. Results guide risk stratification, family screening, and personalised management for individuals with a personal or family history of heart muscle disease.
| Feature | Our TPM1 NGS Test | Broad Cardiomyopathy Panel |
|---|---|---|
| Precision | >99.9% sensitivity for TPM1 coding variants | ~98% per gene; risk of false negatives |
| Methodology | NGS with deep intronic coverage | Standard exon-focused NGS |
| Turnaround | 3–4 weeks | 4–6 weeks |
Physician Insight & Safety Protocols
“A negative TPM1 result does not exclude inherited cardiomyopathy; always correlate findings with echocardiography, ECG, and detailed family history. This test is a powerful tool, not a standalone diagnosis.”
— Lina Osama Zaki Quteineh, Consultant Medical Genetics (DHA Registration ID: 9294403)
Important Medication Safety Advisory
⚠️ Medication Safety
Do not discontinue prescribed medications (e.g., beta-blockers, ACE inhibitors) without consulting your treating cardiologist. Discontinuation may precipitate heart failure or arrhythmia.
Patient Safety: Exclusion Criteria & Emergency Red Flags
- Acute myocardial infarction within the last 4 weeks
- Currently pregnant (requires separate genetic counselling)
- Severe anaemia (Hb < 8 g/dL) – may affect sample quality
- Seek emergency care immediately if you experience sudden chest pain, fainting (syncope), or severe shortness of breath.
- Do not rely on genetic test results alone if symptoms develop; always call emergency services.
Patient FAQ & Clinical Guidance
1. What does the TPM1 genetic test detect and who should consider it?
This next-generation sequencing test identifies mutations in the TPM1 gene that cause dilated cardiomyopathy, recommended for individuals with a family history of cardiomyopathy, early heart failure, or unexplained sudden cardiac death. It clarifies inheritance risk and guides life-saving surveillance.
2. How accurate is the test and when will I receive results?
Our ISO‑accredited NGS protocol delivers 99.9% analytical sensitivity for TPM1 variants; reports are issued within 3–4 weeks from sample receipt, accompanied by a molecular genetics interpretation.
3. Is home blood collection available across the UAE?
Yes, our DHA‑licensed mobile phlebotomy team visits your home or office from 8 AM to 11 PM daily, using cold‑chain transport that preserves DNA integrity; this service is included in the 2800 AED price.
UAE Regulatory & Data Privacy Adherence
Regulatory Compliance
- Data privacy safeguarded under Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL); all patient information encrypted and stored in compliant servers.
- Health data protection aligned with Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields.
- Patient consent and clinical safety conducted in accordance with Federal Decree-Law No. 4 of 2016 on Medical Liability.
- Facility licensed by Dubai Health Authority (DHA) – License No. 1143.
Clinical & Logistical Metadata
| Test Name | TPM1 Gene Cardiomyopathy, Dilated Type 1Y Genetic Test (Next-Generation Sequencing) |
| Price (AED) | 2,800 |
| Turnaround Time | 3–4 weeks (from sample receipt) |
| Sample Type / Matrix | Peripheral whole blood (EDTA tube) |
| Methodology Used | Next-Generation Sequencing (NGS) – whole coding region + flanking intronic regions |
| ICD-10-CM Code | I42.0 (Dilated cardiomyopathy) |
| LOINC Code | 21636-6 (TPM1 gene mutation analysis) |
| DHA Facility License & Laboratory Address | DHA License No: 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