Test Price
2,800 AED✅ Home Collection Available
SCN4B Gene Long QT Syndrome Type 10 Genetic Test in UAE – 2800 AED – DHA Certified
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% diagnostic sensitivity via ISO 9001:2015 accredited next‑generation sequencing.
- Premium Logistics: VIP mobile phlebotomy with temperature‑controlled cold‑chain home collection (8 AM–11 PM daily).
- Clinical Guidance: Telephonic post‑test genetic counseling for result interpretation.
- Insurance: Direct billing verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
This NGS‑based test identifies pathogenic variants in the SCN4B gene, enabling precise diagnosis, risk stratification, and family screening for Long QT syndrome type 10. Full gene coverage at >100x read depth ensures detection of clinically significant variants.
| Feature | Our Test (ISO 9001:2015) | Closest Alternative |
|---|---|---|
| Precision | Full SCN4B gene coverage, >100x read depth | Limited panel or partial exon analysis |
| Methodology | Next‑Generation Sequencing (NGS) with MLPA backup | Sanger sequencing (single gene) |
| Turnaround | 3–4 weeks | 6–8 weeks |
Physician Insight & Safety Protocols
“As a DHA‑licensed Consultant Medical Geneticist, I remind every patient that a genetic test result is one piece of a comprehensive cardiac evaluation. Never make clinical decisions solely on this test; always correlate with ECG, Holter monitoring, and family history under expert supervision.”
— Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
Medication Advisory
⚠️ Important Medication Warning
Do not discontinue prescribed beta‑blockers or antiarrhythmic drugs without consulting your doctor. Abrupt cessation can precipitate life‑threatening arrhythmias in Long QT syndrome. Always discuss any medication changes with your cardiologist.
Exclusion Criteria & Emergency Red Flags
Contraindications for Testing
- Acute myocardial infarction within the past 30 days.
- Uncorrected electrolyte imbalances (potassium, magnesium) – must be normalized before sample collection.
- Poor DNA quality from hemolyzed or clotted blood – recollect if necessary.
- Seek immediate emergency care if you experience syncope, seizure‑like activity, or sustained palpitations while awaiting your results.
Patient FAQ & Clinical Guidance
1. What does the SCN4B genetic test detect?
This test identifies pathogenic DNA variants in the SCN4B gene that cause Long QT syndrome type 10, enabling early risk assessment and targeted family screening.
2. How is the sample collected? Is a hospital visit required?
We offer VIP mobile phlebotomy with cold‑chain transport. A simple blood draw, extracted DNA, or an FTA card sample can be collected at your home, office, or hotel across the UAE. No hospital visit is necessary.
3. What regulations govern data privacy and test accuracy?
This test fully complies with Federal Decree‑Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 concerning health information technology. Clinical safety is governed by Federal Decree‑Law No. 4 of 2016 on Medical Liability. Our laboratory is ISO 9001:2015 certified (Cert: INT/EGQ/2509DA/3139) and operates under DHA facility license 1143.
UAE Regulatory & Data Privacy Adherence
Your data is protected under:
- Federal Decree‑Law No. 45 of 2021 on Personal Data Protection (PDPL) – guarantees your genetic data is collected, processed, and stored with explicit consent and security.
- Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields – ensures secure electronic health information handling.
- Federal Decree‑Law No. 4 of 2016 on Medical Liability – safeguards clinical testing safety and informed consent.
All test results are encrypted and access‑controlled. For inquiries about your data rights, contact our DHA‑registered data protection officer.
Clinical & Logistical Metadata
| Test Name | SCN4B Gene Long QT Syndrome Type 10 Genetic Test |
| Price (AED) | 2,800 |
| Turnaround Time | 3–4 weeks |
| Sample Type / Matrix | Peripheral blood (whole blood, extracted DNA, or FTA card) |
| Methodology Used | Next‑Generation Sequencing (NGS) with MLPA backup |
| ICD-10-CM Code | I45.81 |
| LOINC Code | 92418-9 |
| DHA Facility License & Laboratory Address | DHA License No. 1143, Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE. Lab: DNA Labs UAE |
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Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians