Test Price
2,800 AED✅ Home Collection Available
PPARG Gene Carotid Intimal Medial Thickness Type 1 Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين PPARG للسمك الباطني-الغلالي للشريان السباتي النوع الأول في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
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 and VIP Mobile Phlebotomy available from 8 AM – 11 PM, 7 days a week.
Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation with a DHA-licensed genetic counsellor.
Insurance: Direct Billing Verification via WhatsApp at +971 54 548 8731.
ضمان الدقة: حساسية تشخيصية 99.9% عبر معالجة معتمدة ISO 9001:2015.
الخدمات اللوجستية المتميزة: سحب منزلي بدرجة مستشفى عبر سلسلة تبريد معتمدة ISO، وسحب دموي متنقل VIP.
الإرشاد السريري: استشارة هاتفية بعد الاختبار لتفسير النتائج.
التأمين: التحقق المباشر من الفواتير عبر واتساب +971 54 548 8731.
Test Overview
The PPARG Gene Carotid Intimal Medial Thickness Type 1 Genetic Test is a next-generation sequencing assay that identifies variants in the PPARG gene linked to subclinical atherosclerosis and carotid intimal-medial thickness (CIMT). This analysis empowers precise cardiovascular risk stratification and early intervention for patients and at-risk family members.
| Feature | Our Test (Centers of Clinical Excellence) | Closest Alternative (Standard Labs) |
|---|---|---|
| Precision | >99.9% analytical accuracy with NGS & Sanger confirmation | Genotyping panels with limited variant coverage |
| Method | Next-Generation Sequencing (NGS) of the full PPARG coding region | Single nucleotide polymorphism (SNP) array or targeted genotyping |
| Speed | TAT 3 – 4 Weeks with comprehensive clinical report | Often 6 – 8 weeks without genetic counselling |
*All comparisons are based on 2026 standard-of-care benchmarks.
Physician Insight & Safety Protocol
Dr. PRABHAKAR REDDY (DHA: 61713011) states: “This genetic test is an important step, but it must be interpreted within your full clinical picture. A variant does not determine your destiny – your lifestyle and medical follow-up remain the pillars of vascular health.”
Medication Warning: Do not discontinue any prescribed medication (antiplatelets, statins, antihypertensives) without consulting your doctor. Abrupt changes can precipitate serious vascular events.
Exclusion Criteria & Emergency Red Flags
- Exclusion: Recent blood transfusion (within 4 weeks) may affect DNA quality; notify the phlebotomist.
- Exclusion: Failure to provide informed consent or complete a genetic counselling session prior to blood draw.
- Red Flag: New-onset sudden severe headache, transient vision loss, or one-sided weakness – go to the nearest ER immediately.
- Red Flag: Test results alone are not a diagnosis; urgent symptoms require emergency care regardless of genetic status.
Frequently Asked Questions (FAQ)
1. What exactly does this PPARG genetic test detect, and how accurate is it?
This investigation sequences the entire coding region of the PPARG gene with 99.9% diagnostic sensitivity, identifying DNA variants associated with carotid intimal medial thickness type 1 and heritable vascular risk. It is not a diagnostic for existing atherosclerosis but a susceptibility marker to guide proactive management.
يكتشف هذا الاختبار طفرات جين PPARG بحساسية تشخيصية فائقة، مما يساعد في تقدير المخاطر الوعائية الوراثية وتوجيه التدابير الوقائية.
2. Can I do this test if I am under 18 or need my child tested?
In accordance with UAE CDS Law 2026 regarding minors, genetic testing on individuals below 18 years requires the explicit consent of both parents or legal guardians, and must be accompanied by a pre-test genetic counselling session. Home collection can be arranged for pediatric samples with prior approval.
بموجب قانون الأدوية والسموم المراقبة لعام 2026، يلزم موافقة الوالدين وإجراء استشارة وراثية قبل الاختبار للأفراد دون 18 عامًا.
3. How is my genetic data protected under UAE law?
Your sample and genomic data are protected under the UAE Personal Data Protection Law (PDPL) and Federal Decree-Law No. 41 of 2024 (Art. 87). We adhere to ISO 9001:2015 standards, and all data is anonymized, stored on encrypted servers within the UAE, and never shared without your written consent.
بياناتك الجينية محمية بموجب قانون حماية البيانات الشخصية الإماراتي (PDPL) والمرسوم بقانون اتحادي رقم 41 لسنة 2024، مع تخزين مشفر داخل الدولة.
Pre-Test Requirements & Specimen Collection
- Sample Type: Whole Blood (EDTA tube), Extracted DNA, or Finger-Prick Blood on FTA Card – collected by our VIP mobile phlebotomy team.
- Pre-test Clinical History: Please provide any previous carotid ultrasound reports, family history of premature vascular disease, and current medication list.
- A mandatory Genetic Counselling session will be conducted to draw a pedigree chart and explain the implications of results.
- Turnaround Time: 3 to 4 Weeks from sample receipt at our ISO-certified laboratory.
- Price: 2800 AED (inclusive of counselling, collection, and comprehensive report).
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