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2,800 AED

✅ Home Collection Available

SCN5A Gene Brugada Syndrome Type 1 Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines

تحليل جين SCN5A لمتلازمة بروجادا من النوع الأول في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي

Executive Summary | الخلاصة التنفيذية

دقة تشخيصية 99.9% عبر مختبر معتمد آيزو. 99.9% Diagnostic Sensitivity via ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139) NGS platform.

Premium Logistics: ISO certified cold-chain home collection & VIP mobile phlebotomy, 8 AM–11 PM daily.

Clinical Guidance: Complimentary post‑test teleconsultation with a genetic counselor or cardiologist for result interpretation.

Insurance: Direct billing verification via WhatsApp +971 54 548 8731.

UAE Regulatory Compliance: Federal Decree‑Law No. 41 of 2024 (Art. 87), CDS Law 2026 (Minors), UAE PDPL.

Test Overview & Clinical Utility

This advanced genetic test sequences the entire SCN5A gene using Next Generation Sequencing (NGS) to detect mutations associated with Brugada syndrome type 1 – a life‑threatening cardiac channelopathy causing ventricular arrhythmia and sudden cardiac death. تحليل جيني شامل يكشف طفرات جين SCN5A المسؤولة عن متلازمة بروجادا النوع الأول، ويُوجه استراتيجيات الوقاية والعلاج المبني على المخاطر.

Feature Our NGS Test Closest Alternative (Sanger Panel)
MethodNGS (full gene & intron–exon boundaries)Sanger sequencing of selected exons
Sensitivity>99.9% (incl. deep intronic variants)~95% (misses regulatory/ intronic)
Turnaround3–4 Weeks6–8 Weeks
Price2800 AED2500–3000 AED
Clinical ReportACMG‑classified variants + actionable managementLimited interpretation

Physician Insight & Safety Protocol

“As a Consultant Interventional Cardiologist & Electrophysiologist, I emphasize that this genetic result is one piece of a comprehensive risk assessment. A negative SCN5A finding does not exclude Brugada syndrome; a positive result must be correlated with ECG, Holter monitoring, and family cascade screening. Your personal risk management plan should be developed with your treating cardiologist. Please, never stop prescribed medications without consultation.”

— Dr. PRABHAKAR REDDY, DHA License No. 61713011

⚠️ Medication Safety Warning:

Do not discontinue prescribed antiarrhythmic drugs (e.g., quinidine, beta‑blockers) or any cardiac medication without explicit approval from your physician. Abrupt cessation can trigger malignant arrhythmias.

Patient Safety & Exclusion Criteria

  • Exclusion: Active febrile illness (may alter ECG phenotype); pregnancy – genetic counselling required; minors requiring parental consent per UAE CDS Law 2026.
  • Sample Requirements: Whole blood (EDTA tube), extracted DNA, or one drop on FTA card. Avoid haemolysed samples.
  • Emergency Red Flags – seek immediate medical attention if: syncope, nocturnal agonal respiration, witnessed sudden cardiac arrest, or strong family history of SCD under 45 years.

Patient FAQ & Clinical Guidance

1. What does a positive SCN5A mutation mean for my heart health?

Key Answer: A positive result identifies a likely pathogenic variant in the SCN5A gene, significantly elevating your risk for Brugada syndrome type 1 and sudden cardiac events.

تعني النتيجة الإيجابية تحديد طفرة ممرضة في جين SCN5A تزيد من خطر الإصابة بمتلازمة بروجادا النوع الأول واضطراب النظم القلبي المهدد للحياة.

2. How accurate is this NGS test for Brugada syndrome compared to traditional methods?

Key Answer: With >99.9% analytical sensitivity and full gene coverage, our NGS detects even deep intronic and copy‑number variants missed by standard Sanger sequencing panels.

دقة التحليل تتجاوز 99.9% ويغطي تسلسل الجين بالكامل، مما يلتقط طفرات يصعب اكتشافها بالفحوص التقليدية مثل تسلسل سانغر.

3. Can I have the blood sample collected at home in the UAE?

Key Answer: Yes, our ISO‑certified home collection service operates daily from 8 AM to 11 PM, with cold‑chain transport ensuring sample integrity from your doorstep.

نعم، نقدم خدمة سحب الدم المنزلي المعتمدة آيزو يومياً من 8 صباحاً إلى 11 مساءً مع نقل مبرد للحفاظ على العينة.

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