Test Price
2,800 AED✅ Home Collection Available
MT-ATP8 Gene Genetic Test for Cardiomyopathy, Apical Hypertrophic Cardiomyopathy & Neuropathy in UAE – 2800 AED
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO‑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 result interpretation provided by a DHA‑licensed clinician.
- Insurance: Direct billing verification via WhatsApp at +971 54 548 8731.
This NGS‑based MT-ATP8 gene test delivers definitive molecular results for hereditary cardiomyopathies and neuropathy, supported by accredited logistics and post‑clinical guidance from DNA Labs UAE.
Test Overview & Methodology
This single‑gene NGS test sequences the entire coding region of the MT-ATP8 mitochondrial gene to identify pathogenic and likely pathogenic variants linked to mitochondrial cardiomyopathies, apical hypertrophic cardiomyopathy, and neuropathy with >99.9% analytical sensitivity. The assay employs the Illumina NovaSeq 6000 platform with deep coverage dedicated to MT-ATP8, ensuring detection of variants that multi‑gene panels frequently miss or underrepresent.
Pre‑Test Requirements
- Submit a detailed clinical history including family cardiomyopathy and neuropathy records.
- A mandatory genetic counselling session (in‑clinic or telehealth) to construct a pedigree chart of affected family members.
- Samples accepted: Whole blood (EDTA), extracted DNA, or one drop of blood on an FTA card. No fasting or medication adjustment required.
| Feature | Our Test – MT-ATP8 Full Gene Sequencing | Closest Alternative – Standard Cardiac Panel |
|---|---|---|
| Precision | Single‑gene deep coverage; >99.9% analytical sensitivity for MT-ATP8 (NGS) | Multi‑gene panel; MT-ATP8 often excluded or shallow coverage |
| Method | Next‑Generation Sequencing (Illumina NovaSeq 6000 platform) | NGS with variable bioinformatics; may miss mitochondrial variants |
| Turnaround Time | 3 – 4 Weeks | 4 – 8 Weeks (often outsourced) |
Physician Insight & Safety Protocols
“The MT-ATP8 genetic result must be correlated with a thorough clinical evaluation – a variant of uncertain significance should never be mistaken for a definitive diagnosis. I urge every patient to discuss findings with their cardiologist or neurologist before any treatment change. Genetics informs, but clinical judgement guides.” – Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
Medication Advisory
⚠️ Do Not Discontinue Prescribed Medication Without Consulting Your Doctor
Always seek direct medical advice before altering any treatment regimen based on genetic findings. Genetic test results complement, but do not replace, professional clinical judgement.
Exclusion Criteria & Emergency Red Flags
- Acute chest pain, syncope, severe palpitations, or sudden muscle weakness require immediate Emergency Room attendance – do not wait for genetic test results.
- This test is not designed for prenatal diagnosis or predictive testing in asymptomatic minors without specialist counselling.
- Minors under 18 years must provide guardian consent as per UAE Federal Law No. 2 of 2019; unaccompanied minors will not be sampled.
Patient FAQ & Clinical Guidance
1. What exactly does the MT-ATP8 gene test detect?
This NGS test sequences the entire coding region of the MT-ATP8 mitochondrial gene to identify mutations causing hereditary cardiomyopathies and neuropathy. It provides a definitive molecular diagnosis for apical hypertrophic cardiomyopathy and associated neurological conditions.
2. Can I give a blood sample at home, and how long does the result take?
Yes, our VIP mobile phlebotomy team collects blood or a finger‑prick FTA card at your doorstep daily from 8 AM to 11 PM. Results are delivered within 3 to 4 weeks from sample receipt at the laboratory.
3. Will my insurance cover the 2800 AED cost for this genetic test?
Many UAE insurers reimburse genetic testing when medically necessary. We verify your coverage directly via WhatsApp before scheduling your appointment to ensure transparency with no hidden costs.
4. Do I need to fast or adjust my medications before the blood draw?
No special fasting or medication adjustment is required. A standard whole blood sample in an EDTA tube, extracted DNA, or a dried blood spot on an FTA card is sufficient for analysis.
UAE Regulatory & Data Privacy Adherence
Your Test is Protected by UAE Law
- Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) – all genomic data is handled with full encryption and stored locally in compliance with UAE data protection regulations.
- Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields – governs the secure digital transmission and storage of your health information and test results.
- Federal Decree-Law No. 4 of 2016 on Medical Liability – ensures clinical testing safety and mandates informed patient consent for all genetic analyses.
- ISO 9001:2015 Certified – Certificate INT/EGQ/2509DA/3139, ensuring quality management across all laboratory processes.
Clinical & Logistical Metadata
| Test Name | MT-ATP8 Gene Genetic Test (Cardiomyopathy & Neuropathy Panel) |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3 – 4 Weeks |
| Sample Type / Matrix | Whole Blood (EDTA), Extracted DNA, or FTA Card – VIP Mobile Phlebotomy & Temperature‑Controlled Cold‑Chain Home Collection Available Daily 8 AM – 11 PM |
| Methodology Used | Next‑Generation Sequencing (NGS) – Illumina NovaSeq 6000 |
| ICD-10-CM Code | I42.2, G60.9 |
| LOINC Code | 81258-9 |
| 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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Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians