Test Price
2,800 AED✅ Home Collection Available
MT-TY Gene NGS Test for FSGS & Dilated Cardiomyopathy in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين MT-TY لتشخيص التصلب الكبيبي القطعي البؤري واعتلال عضلة القلب التوسعي في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Clinical Excellence & UAE Compliance Snapshot
ملخص تنفيذي: يقدم مركزنا تحليل جين MT-TY بتقنية تسلسل الجيل التالي (NGS) بدقة تشخيصية 99.9%، مع خدمة سحب منزلي متميزة ومطابقة للمعايير الصحية في دبي وضمان خصوصية البيانات.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection & VIP Mobile Phlebotomy (8 AM – 11 PM).
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation by DHA-licensed specialists.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Comparative Edge
The MT-TY gene test employs Next‑Generation Sequencing (NGS) to identify pathogenic variants associated with focal segmental glomerulosclerosis (FSGS) and dilated cardiomyopathy (DCM). This analysis provides a definitive molecular diagnosis in 3–4 weeks, far surpassing conventional single‑gene panels in resolution and clinical relevance.
| Feature | Our MT-TY NGS Test | Closest Alternative (Single-Gene Sanger) |
|---|---|---|
| Precision | 99.9% Sensitivity, full gene coverage (exons ±20bp) | 95% Sensitivity, limited to known hotspots |
| Methodology | NGS (Illumina platform) with clinically validated bioinformatics | Sanger Sequencing (single amplicon) |
| Turnaround Time | 3–4 Weeks | 4–6 Weeks (often batched) |
| Price | 2800 AED | ~3500 AED |
Physician Insight & Safety Protocol
“I advise every patient and family to interpret this genetic result within the full clinical context. A negative result does not exclude disease, and a positive result requires multidisciplinary management. Please continue all prescribed medications and follow your physician’s guidance carefully.” – Dr. PRABHAKAR REDDY (DHA: 61713011)
Do not discontinue prescribed medication without consulting your doctor. Genetic test results are not a substitute for ongoing clinical care.
Exclusion Criteria & ER Red Flags- Test cannot be performed on unlabelled or haemolysed samples – recollection required.
- Acute decompensated heart failure or rapid renal function decline are not contraindications, but immediate emergency care must take priority.
- If patient develops syncope, severe chest pain, or anuria, seek emergency medical attention and postpone elective testing.
Patient FAQ & Clinical Guidance
What is the MT-TY gene test and how does it work?
The MT-TY gene test uses Next‑Generation Sequencing to detect mutations linked to FSGS and dilated cardiomyopathy, providing a definitive molecular diagnosis in 3–4 weeks. It analyses the entire coding region of the mitochondrial MT-TY gene from a blood sample or extracted DNA, identifying pathogenic variants responsible for these inherited conditions.
How is the sample collected and what preparation is required?
Our certified phlebotomist arrives at your home or office between 8 AM and 11 PM, using a cold‑chain transport system that preserves DNA integrity from vein to laboratory. No fasting is needed; you must provide a clinical history and a completed genetic counselling pedigree (before sample collection). The accepts whole blood, extracted DNA, or a single drop on an FTA card.
هل الاختبار مناسب للأطفال وهل يتطلب موافقة الوالدين؟
بموجب القانون الاتحادي الإماراتي رقم 41 لسنة 2024 (المادة 87) وقانون حماية البيانات الشخصية، يلزم الحصول على موافقة صريحة من ولي الأمر قبل سحب عينة من القاصر. الاختبار متاح للأطفال عند الاشتباه السريري بوجود FSGS أو اعتلال عضلة القلب التوسعي الوراثي، ويشترط تقديم رسم شجرة العائلة من جلسة الاستشارة الوراثية.
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