KCNQ1 Gene Long QT syndrome type 1 Genetic Test sale cost 4400 AED
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KCNQ1 Gene Long QT syndrome type 1 Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The KCNQ1 Gene Long QT Syndrome Type 1 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the KCNQ1 gene, which are associated with Long QT Syndrome Type 1 (LQTS1). LQTS1 is a rare inherited heart condition that can lead to irregular heartbeats, fainting, and sudden death due to its influence on the heart’s electrical activity. The test involves analyzing the patient’s DNA to detect any genetic abnormalities in the KCNQ1 gene, which plays a crucial role in the proper function of heart cells.

By identifying specific mutations in the KCNQ1 gene, healthcare providers can better understand an individual’s risk for developing LQTS1, enabling them to implement personalized treatment plans and preventive measures. This can include lifestyle adjustments, medication, or even surgery, depending on the severity of the condition and the patient’s overall health.

The test is priced at 4400 AED and is conducted at DNA Labs UAE, a leading facility known for its advanced genetic testing services. The cost reflects the comprehensive nature of the test, including the sophisticated technology and expertise required to accurately identify and interpret genetic mutations associated with Long QT Syndrome Type 1. For individuals with a family history of LQTS or unexplained cardiac events, this test can be a critical step towards ensuring a healthier future.

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KCNQ1 Gene Long QT syndrome type 1 Genetic Test

At DNA Labs UAE, we offer the KCNQ1 Gene Long QT syndrome type 1 Genetic Test to diagnose and manage Long QT syndrome type 1 (LQT1), a genetic disorder that affects the heart’s electrical system.

Test Components

  • Price: 4400.0 AED

Sample Condition

We accept blood samples, extracted DNA samples, or one drop of blood on an FTA Card for this test.

Report Delivery

Test results are typically delivered within 3 to 4 weeks.

Method

We use NGS (Next-Generation Sequencing) technology for this genetic test.

Test Type

This test is classified under Cardiovascular Pneumology Disorders.

Doctor

A cardiologist will oversee the KCNQ1 Gene Long QT syndrome type 1 Genetic Test.

Test Department

This test is conducted by our Genetics department.

Pre Test Information

Prior to the test, we recommend a genetic counseling session to gather the clinical history of the patient and to draw a pedigree chart of family members affected by KCNQ1 Gene Long QT syndrome type 1.

Test Details

The KCNQ1 gene is associated with Long QT syndrome type 1 (LQT1), a genetic disorder that causes abnormalities in the heart’s electrical system. This can result in prolonged QT intervals on an electrocardiogram (ECG), leading to potentially life-threatening arrhythmias.

Our NGS genetic testing technique allows for the simultaneous analysis of multiple genes, including the KCNQ1 gene. By analyzing a DNA sample obtained from blood or saliva, we can identify any variations or mutations in the KCNQ1 gene that are known to be associated with LQT1.

If a mutation is found, it can help confirm a diagnosis of LQT1 and guide treatment decisions, such as medication options or the need for implantable cardioverter-defibrillator (ICD) placement.

It is important to note that genetic testing for LQT1 is typically recommended for individuals with a personal or family history of prolonged QT intervals or sudden cardiac death. The test results should be interpreted by a healthcare professional with expertise in genetics and cardiovascular medicine.

Test Name KCNQ1 Gene Long QT syndrome type 1 Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Cardiovascular Pneumology Disorders
Doctor Cardiologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for KCNQ1 Gene Long QT syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with KCNQ1 Gene Long QT syndrome type 1 NGS Genetic DNA Test gene KCNQ1
Test Details

The KCNQ1 gene is associated with Long QT syndrome type 1 (LQT1), which is a genetic disorder that affects the heart’s electrical system. LQT1 is characterized by a prolonged QT interval on an electrocardiogram (ECG), which can lead to abnormal heart rhythms and potentially life-threatening arrhythmias.

NGS (Next-Generation Sequencing) is a genetic testing technique that allows for the simultaneous analysis of multiple genes, including the KCNQ1 gene, to identify any variations or mutations that may be present. This type of genetic testing can provide valuable information for diagnosing and managing LQT1.

The KCNQ1 gene NGS genetic test involves obtaining a DNA sample, usually through a blood sample or saliva sample, and analyzing it using NGS technology. The test looks for variations or mutations in the KCNQ1 gene that are known to be associated with LQT1. If a mutation is identified, it can help confirm a diagnosis of LQT1 and guide treatment decisions, such as medication options or the need for implantable cardioverter-defibrillator (ICD) placement.

It is important to note that genetic testing for LQT1 is typically recommended for individuals who have a personal or family history of prolonged QT intervals or sudden cardiac death. The test results should be interpreted by a healthcare professional with expertise in genetics and cardiovascular medicine.

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