What sample type is required for this test?

We accept peripheral whole blood collected in an EDTA tube or a DNA sample collected on an FTA card. Ensure proper collection and handling procedures are followed.

What does the test detect?

The test detects pathogenic variants, including single nucleotide variants (SNVs), insertions/deletions (indels), and copy number variants (CNVs) within the KCNQ1 gene.

Molecular Diagnostics → Genetic Cardiac

Results: 3–4 Weeks Sample: Peripheral whole blood (EDTA) or FTA card

Test Price

2,800 AED

✅ Home Collection Available

📋 Results in 3–4 Weeks

KCNQ1 Gene Long QT Syndrome Type 1 Genetic Test in UAE – 2800 AED

Q: How does the KCNQ1 NGS test work?

This NGS test sequences all exons of the KCNQ1 gene, detecting point mutations, deletions, and duplications with 99.9% accuracy. It provides comprehensive coverage of coding regions and splice sites for reliable diagnosis of Long QT syndrome type 1.

Q: What is the turnaround time for results?

Results are delivered within 3 to 4 weeks, utilizing robust ISO-certified bioinformatics pipelines for variant interpretation and medical review.

Q: Can I use insurance to cover the cost?

We verify insurance via WhatsApp (+971 54 548 8731), providing direct billing to major UAE insurers for seamless payment. Coverage is subject to your policy terms.

Executive Summary & Core Metrics

This advanced genetic test utilises next-generation sequencing (NGS) to detect pathogenic variants in the KCNQ1 gene, providing diagnostic accuracy exceeding 99.9% for Long QT syndrome type 1. Our service includes ISO-certified sample processing, post-test clinical guidance, and direct insurance billing for a seamless patient experience.

Accuracy Guarantee: 99.9% diagnostic sensitivity via ISO-accredited NGS methodology.
Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Available daily from 8 AM to 11 PM).
Clinical Guidance: Telephonic post-test consultation for result interpretation and management recommendations.
Insurance: Direct billing verification via WhatsApp +971 54 548 8731.

Test Overview & Methodology

The KCNQ1 Gene Long QT Syndrome Type 1 Genetic Test employs comprehensive next-generation sequencing covering all exons, splice sites, and copy number variants within the KCNQ1 gene. This test is essential for diagnosing inherited long QT syndrome type 1, a condition that predisposes individuals to life-threatening cardiac arrhythmias. Early detection through this NGS platform enables targeted therapeutic interventions such as beta-blockade and lifestyle modifications.

Feature	Our KCNQ1 NGS Test	Closest Alternative (Sanger Sequencing)
Methodology	NGS covering all exons, splice sites, and CNVs	Sanger sequencing of coding regions only
Turnaround Time	3–4 Weeks	4–6 Weeks
Detection Rate for KCNQ1 Mutations	>99.9% sensitivity for SNVs and indels	~98% sensitivity for point mutations
Copy Number Variant Detection	Included	Not routinely included
Price	2800 AED	Often higher

Physician Insight & Safety Protocols

"Long QT syndrome type 1 is a serious yet manageable condition when detected early. Our NGS test empowers clinicians with precise genetic information to guide life-saving therapy, including beta-blockade and lifestyle modifications. Always correlate genetic findings with clinical presentation and family history for optimal care." – Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403

Advisory: Medication Safety

⚠️ Medication Warning

Do not discontinue prescribed medication without consulting your doctor.

Exclusion Criteria & Emergency Red Flags

Exclusion: Recent blood transfusion (<4 weeks) or bone marrow transplant within last 3 months may interfere with genetic analysis.
Exclusion: Sample collection for DNA on FTA card requires strict handling; contact our team for instructions.
ER Red Flag: Sudden onset palpitations, syncope (fainting), or family history of sudden unexplained death while awaiting results warrants immediate cardiac evaluation.

Patient FAQ & Clinical Guidance

1. How does the KCNQ1 NGS test work?

This NGS test sequences all exons of the KCNQ1 gene, detecting point mutations, deletions, and duplications with 99.9% accuracy. It provides comprehensive coverage of coding regions and splice sites for reliable diagnosis of Long QT syndrome type 1.

2. What is the turnaround time for results?

Results are delivered within 3 to 4 weeks, utilizing robust ISO-certified bioinformatics pipelines for variant interpretation and medical review.

3. Can I use insurance to cover the cost?

We verify insurance via WhatsApp (+971 54 548 8731), providing direct billing to major UAE insurers for seamless payment. Coverage is subject to your policy terms.

UAE Regulatory & Data Privacy Adherence

Regulatory Compliance: This genetic testing service is performed at a DHA-certified facility (License No. 1143) located at Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE. All operations adhere to Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. Clinical safety and patient consent follow Federal Decree-Law No. 4 of 2016 on Medical Liability. Patient data is handled under strict confidentiality with ISO 9001:2015 certified protocols (Cert: INT/EGQ/2509DA/3139).

Clinical & Logistical Metadata

Test Name	KCNQ1 Gene Long QT Syndrome Type 1 Genetic Test
Price (AED)	2800 AED
Turnaround Time	3–4 Weeks
Sample Type / Matrix	Peripheral whole blood (EDTA) or FTA card
Methodology Used	Next-Generation Sequencing (NGS) covering all exons, splice sites, and CNVs
ICD-10-CM Code	I45.81 (Long QT syndrome)
LOINC Code	96543-7
DHA Facility License & Address	License No. 1143 \| Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE

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Medically Reviewed by Dr. Lina Osama Zaki Quteineh

All content reviewed by qualified professionals for accuracy.

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ISMS 27001:2022

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ISO Accredited

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HIPAA

All reports reviewed by DHA-Certified physicians