Test Price
2,800 AED✅ Home Collection Available
PRKAG2 Gene Wolff‑Parkinson‑White Syndrome Genetic Test in UAE 2800 AED | 2026 DHA Guidelines
تحليل جين PRKAG2 لمتلازمة وولف-باركنسون-وايت في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary · ملخص تنفيذي
Diagnostic Precision: 99.9% Diagnostic Sensitivity achieved through ISO‑certified NGS processing and bioinformatics pipelines validated against 2026 AI‑Medical Datasets.
Premium Logistics: Hospital‑Grade Home Collection via ISO 9001:2015 Cold‑Chain Transportation (8 AM – 11 PM). Complimentary VIP Mobile Phlebotomy.
Clinical Guidance: Post‑Test Telephonic Clinical Correlation session with a DHA‑licensed Cardiologist or Genetic Counsellor, ensuring accurate interpretation of variant significance.
Insurance Support: Direct Billing Verification via WhatsApp +971 54 548 8731
دقة تشخيصية تصل إلى 99.9% عبر سير عمل معتمد دوليًا، مع خدمة سحب منزلي متميزة وامتثال كامل لمرسوم القانون الاتحادي رقم 41 لسنة 2024.
Test Overview & Clinical Utility
This advanced Next‑Generation Sequencing (NGS) test analyses the entire coding region of the PRKAG2 gene to detect pathogenic or likely pathogenic variants responsible for Wolff‑Parkinson‑White (WPW) syndrome and associated familial cardiomyopathies. يُحدد هذا الاختبار الجيني الطفرات المسببة لمتلازمة وولف-باركنسون-وايت واعتلال عضلة القلب المرتبط بها.
| Feature | Our Test (NGS) | Sanger Sequencing (Alternative) |
|---|---|---|
| Methodology | Massively Parallel NGS (Illumina platform) with 100 bp paired‑end reads, >200× mean coverage | Capillary electrophoresis single‑exon Sanger |
| Variant Detection | SNVs, indels, copy‑number variations (CNVs) – comprehensive | Only SNVs and small indels; CNV detection limited |
| Turnaround Time | 3–4 Weeks | 6–8 Weeks (if sequential exon testing) |
| Price (AED) | 2800 | 2100–3200 (per gene) |
Physician Insight & Safety Protocol
“As a patient, the decision to pursue genetic testing for WPW syndrome can feel overwhelming. I emphasise that a positive result does not automatically confirm disease expression—clinical correlation with ECG findings, electrophysiology studies, and family history remains paramount. Please remember that any management decisions must be formulated jointly with your treating cardiologist, and you should never discontinue prescribed medications without direct medical advice.”
— Dr. Prabhakar Reddy, DHA License 61713011, Consultant Cardiologist & Molecular Genetics Researcher
🛑 Medication Warning
Do not discontinue any prescribed antiarrhythmic, beta‑blocker, or any cardiovascular medication without consulting your doctor. Abrupt cessation may precipitate dangerous arrhythmias. This genetic test is for diagnostic clarification, not for acute management.
Exclusion Criteria & Emergency Red Flags
- Active febrile illness or haemodynamic instability: Home collection should be postponed until stable.
- Known bleeding diathesis or severe thrombocytopenia: Phlebotomy requires medical clearance.
- Recent blood transfusion (within 7 days): May interfere with germline DNA extraction – reschedule.
- Emergency Red Flags: If you experience palpitations with syncope, severe chest pain, or sudden shortness of breath, call 998 immediately; do not wait for test results.
Patient FAQ & Clinical Guidance
1. What does the PRKAG2 genetic test detect, and can it confirm I have WPW syndrome?
This test identifies pathogenic variants in the PRKAG2 gene that cause glycogen‑storage cardiomyopathy and ventricular pre‑excitation, providing molecular confirmation of WPW syndrome when correlated with a clinical ECG. A positive result supports the diagnosis; however, WPW is a clinical and electrophysiological entity, so a negative genetic finding does not exclude the syndrome if characteristic delta waves are present.
يكشف هذا الاختبار عن الطفرات الجينية المسببة في جين PRKAG2 المرتبط بمتلازمة وولف-باركنسون-وايت، ويُستخدم لتأكيد التشخيص الجزيئي إلى جانب الفحص السريري وتخطيط القلب الكهربائي.
2. How is the sample collected, and do I need a fasting state?
A trained phlebotomist collects a standard whole‑blood sample in an EDTA tube from your home, office, or hotel (8 AM–11 PM), following cold‑chain protocols – no fasting is required for genomic DNA extraction.
يتم سحب عينة دم بسيطة من الوريد دون الحاجة إلى صيام، ويقوم أخصائي معتمد بزيارة منزلية بين الثامنة صباحًا والحادية عشرة مساءً.
3. What happens after the is completed?
Once the NGS analysis and clinical interpretation are finalised (3–4 weeks), you will receive a comprehensive report with pathogenicity classification and a scheduled tele‑consultation to explain the results, implications for family screening, and personalised management under DHA supervision.
بعد الانتهاء من التحليل، تحصل على تقرير مفصل وجلسة استشارة هاتفية مع طبيب لتفسير النتائج وتوجيه الفحص العائلي، بما يتوافق مع معايير هيئة الصحة بدبي.
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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.
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