Test Price
2,800 AED✅ Home Collection Available
KCNE1 Gene Long QT Syndrome Type 5 Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل KCNE1 الجيني لمتلازمة كيوت الطويلة النوع الخامس في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary – One‑Stop Genetic Risk Assessment for Long QT Syndrome 5
- ✓ 99.9% Diagnostic Sensitivity – ISO‑accredited NGS analysis with variant interpretation per ACMG guidelines.
- ✓ Premium Home Collection – Hospital‑grade cold‑chain logistics for blood, extracted DNA, or FTA card; secure phlebotomy 8 AM‑11 PM.
- ✓ Telephonic Post‑Test Guidance – Expert clinical interpretation of results with a specialist genetic counsellor.
- ✓ Direct Insurance Verification – WhatsApp +971 54 548 8731 for instant eligibility check before sampling.
فحص جيني شامل لجين KCNE1 باستخدام تقنية التسلسل الجيني عالي الإنتاجية للكشف عن الطفرات المسببة لمتلازمة QT الطويلة من النوع الخامس، مع ضمان دقة عالية وامتثال كامل للوائح الصحية في دولة الإمارات.
Overview of the Test
The KCNE1 Gene Long QT Syndrome Type 5 Genetic Test is a targeted molecular diagnostic that screens for pathogenic variants in the KCNE1 gene associated with inherited cardiac arrhythmia. This test empowers cardiologists, geneticists, and informed individuals to clarify personal risk, guide therapy, and initiate family cascade screening with a simple blood or buccal sample.
يساعد هذا التحليل المتطور في تشخيص متلازمة كيوت الطويلة من النوع الخامس وتحديد الأفراد المعرضين للخطر داخل الأسرة.
Test at a Glance
| Aspect | Our Test | Closest Alternative |
|---|---|---|
| Precision | Targeted NGS with complete KCNE1 coverage, variant validation via Sanger | Whole-exome sequencing (incidental findings possible, lower depth) |
| Methodology | ISO‑certified Illumina NGS platform, bioinformatic ACMG classification | Research‑grade panels or older Sanger‑only approaches |
| Turnaround | 3‑4 Weeks with pre‑ and post‑test genetic counselling | 6‑10 Weeks, often without integrated counselling |
| Logistics | Home collection by certified phlebotomist, cold chain, FTA card option | Clinic visit required; limited sample stability |
Physician Insight & Safety Protocol
“Understanding your genetic predisposition to Long QT syndrome is a courageous first step. Our laboratory delivers definitive molecular data, but every result must be correlated with a full cardiac evaluation by your cardiologist. I urge you to continue all prescribed medications and discuss any lifestyle changes with your doctor before acting on genetic findings.”
— Dr. PRABHAKAR REDDY, DHA License No. 61713011
Critical Medication Notice
Do not discontinue any prescribed medication, especially beta‑blockers or anti‑arrhythmics, without consulting your treating physician. Abrupt changes can trigger life‑threatening arrhythmias.
Exclusion Criteria & Emergency Red Flags
- • This test is not a substitute for emergency cardiac care. If you experience chest pain, syncope (fainting), or fast/irregular palpitations, call 998 immediately.
- • Not suitable for individuals without prior clinical assessment for Long QT syndrome symptoms or family history.
- • Minors (<18 years) require legally authorised guardian consent and a referral from a paediatric cardiologist per UAE CDS Law 2026.
- • Patients currently hospitalised for acute arrhythmic events should postpone genetic testing until stabilised.
Patient FAQ & Clinical Guidance
1. What does the KCNE1 gene test detect, and who should consider it?
Expert Snippet: The test identifies inherited mutations in KCNE1 linked to Long QT syndrome type 5, enabling precise risk stratification and family screening.
This test is recommended for individuals with a personal or family history of unexplained syncope, sudden cardiac arrest, or prolonged QT interval on ECG, as well as for cascade testing of relatives after a positive diagnosis.
السؤال: ما الذي يكشف عنه تحليل جين KCNE1 ومن يجب أن يخضع له؟
يكشف التحليل عن طفرات وراثية في جين KCNE1 تسبب متلازمة كيوت الطويلة من النوع الخامس، مما يساعد في تقييم المخاطر وفحص الأقارب.
2. How is the sample collected and what preparation is needed?
Expert Snippet: A certified phlebotomist collects a blood sample, extracted DNA, or a simple finger‑prick on an FTA card during a scheduled home visit.
No fasting is required. A mandatory pre‑test genetic counselling session is conducted to document clinical history and draw a detailed pedigree. The sample remains stable in our cold‑chain transport system until processing.
السؤال: كيف يتم جمع العينة وما هي التحضيرات المطلوبة؟
يقوم أخصائي سحب دم معتمد بجمع العينة منزلياً (دم، DNA مستخلص، أو بقعة دم على بطاقة FTA)، بعد جلسة استشارة جينية.
3. Will I receive genetic counselling along with my results?
Expert Snippet: Yes, our service includes both pre‑ and post‑ counselling with a licensed genetic counsellor to explain findings and implications.
After the laboratory analysis, a personalised telephonic session explains your variant report, its clinical relevance, and next steps for family members. A written, DHA‑compliant report is provided.
السؤال: هل سيتم تقديم استشارة جينية بعد النتائج؟
نعم، تشمل الحزمة جلسة استشارة جينية قبل وبعد الفحص مع مستشار وراثي مرخص لتفسير النتائج وتوجيه الخطوات التالية.
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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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All reports reviewed by DHA-Certified physicians