Test Price
2,800 AED✅ Home Collection Available
MT‑TM Gene‑Related Mitochondrial Myopathy NGS Test in UAE | 2800 AED
Executive Summary & Core Metrics
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 (Daily 8 AM – 11 PM). Hospital‑grade sample handling with ISO certified cold‑chain transport.
-
✓
Clinical Guidance: Complimentary Telephonic Post‑Test Genetic Counselling & Result Interpretation.
-
✓
Insurance & Billing: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test provision is 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 follow Federal Decree‑Law No. 4 of 2016 on Medical Liability.
Test Overview & Methodology
This advanced NGS test sequences the entire MT‑TM mitochondrial gene to detect pathogenic variants linked to mitochondrial myopathy and potentially associated cardiomyopathy. The assay provides comprehensive coverage of coding and flanking regions, enabling identification of both known and novel variants with high diagnostic yield.
| Feature | Our Test (MT‑TM NGS) | Closest Alternative (Sanger Sequencing) |
|---|---|---|
| Methodology | Full‑gene Next‑Generation Sequencing with coverage >99% | Targeted mutation analysis by Sanger sequencing |
| Detection Scope | All known & novel variants in MT‑TM (coding + flanking regions) | Only pre‑specified known mutations |
| Turnaround Time | 3–4 weeks from sample receipt | 4–6 weeks, limited by primer design |
| Clinical Utility | Comprehensive diagnosis, family screening & genetic counselling | Confirmation of previously identified familial mutation only |
Physician Insight & Safety Protocols
Message from Lina Osama Zaki Quteineh, Consultant Medical Genetics (DHA License: 9294403)
Mitochondrial genetic testing yields powerful diagnostic information, yet results must always be interpreted within the full clinical context. I advise every patient to review their report with a certified genetic counsellor before making any medical decisions. This test provides a molecular foundation, but a comprehensive clinical evaluation remains essential for accurate diagnosis and management.
Important Clinical Advisory
Do not discontinue prescribed medication without consulting your doctor. Altering your treatment plan without medical supervision may lead to serious cardiac or metabolic decompensation.
Safety Exclusion Criteria & Emergency Red Flags
- Exclusion criteria: acute febrile illness, inability to provide a blood or DNA sample, lack of a clinical indication for mitochondrial myopathy testing.
- Absolute contraindication: genetic testing requested for a minor without documented legal guardian consent as required by UAE Federal Law.
- Emergency red flags – seek immediate medical attention: sudden severe muscle weakness, breathing difficulty, chest pain, palpitations, or loss of consciousness. These may signal acute mitochondrial crisis or cardiac involvement.
- Home collection is postponed if the patient presents with any exclusion criterion; rescheduling is free of charge.
Patient FAQ & Clinical Guidance
1. What is MT‑TM gene‑related mitochondrial myopathy?
MT‑TM gene mutations cause mitochondrial myopathy, leading to progressive muscle weakness and possible cardiomyopathy detectable by NGS. The disorder affects energy production in muscle cells, often presenting with exercise intolerance, fatigue, and in some patients, cardiac conduction abnormalities. Our NGS test sequences the entire MT‑TM gene to identify pathogenic variants, enabling precise diagnosis and family risk assessment.
2. How is the NGS test performed and what samples are accepted?
A small blood sample, extracted DNA, or a single drop of blood on an FTA card is all that is required. Our phlebotomist collects the sample during a scheduled home visit using cold‑chain transport. The laboratory then extracts DNA and uses Next‑Generation Sequencing to read every nucleotide of the MT‑TM gene, comparing it against reference sequences to detect clinically significant variants.
3. What will the results tell me and is genetic counselling included?
Your report will indicate if a disease‑causing MT‑TM variant is present, absent, or of uncertain significance, with genetic counselling included. A definite pathogenic finding confirms the diagnosis and helps guide family screening. Variants of uncertain significance (VUS) require clinical correlation and may be reclassified as more data emerge. A complimentary post‑test tele‑counselling session with a certified genetic counsellor is provided to explain every detail.
UAE Regulatory & Data Privacy Adherence
All services at DNA Labs UAE are delivered in strict compliance 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 are governed by Federal Decree‑Law No. 4 of 2016 on Medical Liability. Your genetic data is handled with the highest security standards and is never shared without your explicit written consent.
Clinical & Logistical Metadata
| Test Name | MT‑TM Gene‑Related Mitochondrial Myopathy NGS Test |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3–4 weeks from sample receipt |
| Sample Type / Matrix | Peripheral whole blood, extracted DNA, or FTA card specimen |
| Methodology Used | Next‑Generation Sequencing (NGS) with full‑gene coverage >99% |
| ICD-10-CM Code | G71.3 |
| LOINC Code | 81313-5 |
| DHA Facility License & Address | License No. 1143 — Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
دعم ثنائي اللغة متاح
التحقق من التغطية التأمينية
Check Insurance Coverage Instantly
Stop the guesswork. Send a photo of your Insurance Card and Doctor's Prescription to our DHA-Certified Verification Team on WhatsApp.
توقف عن التخمين. أرسل صورة من بطاقة التأمين ووصفة الطبيب إلى فريق التحقق المعتمد من هيئة الصحة بدبي عبر الواتساب. احصل على تحديث الحالة في دقائق.
Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians