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KCNE1 Gene Long QT syndrome type 5 Genetic Test Cost

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

-21%

The KCNE1 Gene Long QT Syndrome Type 5 Genetic Test is a specialized diagnostic examination offered at DNA Labs UAE, designed to detect mutations in the KCNE1 gene, which are associated with Long QT Syndrome Type 5 (LQTS5). LQTS5 is a rare genetic disorder that affects the heart’s electrical activity, leading to potentially life-threatening arrhythmias and sudden cardiac arrest. The test involves analyzing the patient’s DNA to identify specific genetic alterations in the KCNE1 gene that can disrupt the normal heart rhythm.

Given the critical nature of the condition, this genetic test is an essential tool for individuals with a family history of Long QT Syndrome or unexplained cardiac events. Early detection through this test can facilitate timely intervention and management strategies to mitigate the risk of severe complications.

The cost of the KCNE1 Gene Long QT Syndrome Type 5 Genetic Test at DNA Labs UAE is set at 4400 AED. This investment covers the comprehensive analysis required to accurately identify the presence of genetic mutations associated with the condition. The test is conducted by experienced professionals in a state-of-the-art facility, ensuring reliable and precise results for patients seeking clarity about their genetic risk for Long QT Syndrome Type 5.

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KCNE1 Gene Long QT Syndrome Type 5 Genetic Test

At DNA Labs UAE, we offer the KCNE1 Gene Long QT syndrome type 5 Genetic Test. This test helps in diagnosing Long QT syndrome type 5 (LQT5), a cardiac disorder characterized by abnormal heart rhythms.

Test Components

The KCNE1 Gene Long QT syndrome type 5 Genetic Test includes the following 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

Before undergoing the KCNE1 Gene Long QT syndrome type 5 Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session is conducted to draw a pedigree chart of family members affected by the KCNE1 Gene Long QT syndrome type 5 NGS Genetic DNA Test gene KCNE1.

Test Details

The KCNE1 gene is associated with Long QT syndrome type 5 (LQT5). This cardiac disorder is caused by mutations in the KCNE1 gene, which encodes a protein that regulates the electrical activity of the heart.

The KCNE1 Gene Long QT syndrome type 5 Genetic Test uses Next-Generation Sequencing (NGS) technology. NGS is a high-throughput genetic testing method that allows for the simultaneous sequencing of multiple genes. In the case of LQT5, NGS is used to analyze the entire coding region of the KCNE1 gene to identify any mutations or variants.

To perform the KCNE1 Gene Long QT syndrome type 5 Genetic Test, a sample of DNA is obtained. This can be done through a blood sample or a cheek swab. The DNA is then sequenced using NGS technology, and the resulting data is analyzed to identify any mutations or variants in the KCNE1 gene.

This genetic test is useful in diagnosing LQT5 and determining the specific mutation present in an individual. It can also be used for carrier testing in family members of affected individuals and for prenatal testing in families with a known KCNE1 gene mutation.

It is important to note that genetic testing for LQT5 should be performed and interpreted by a qualified healthcare professional, such as a genetic counselor or a medical geneticist. They can provide appropriate counseling and guidance based on the test results.

Test Name KCNE1 Gene Long QT syndrome type 5 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 KCNE1 Gene Long QT syndrome type 5 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with KCNE1 Gene Long QT syndrome type 5 NGS Genetic DNA Test gene KCNE1
Test Details

The KCNE1 gene is associated with Long QT syndrome type 5 (LQT5), which is a cardiac disorder characterized by abnormal heart rhythms. LQT5 is caused by mutations in the KCNE1 gene, which encodes a protein that regulates the electrical activity of the heart.

NGS (Next-Generation Sequencing) is a high-throughput genetic testing method that allows for the simultaneous sequencing of multiple genes. In the case of LQT5, NGS can be used to analyze the entire coding region of the KCNE1 gene to identify any mutations or variants that may be present.

A KCNE1 gene NGS genetic test involves obtaining a sample of DNA, typically through a blood sample or a cheek swab. The DNA is then sequenced using NGS technology, and the resulting data is analyzed to identify any mutations or variants in the KCNE1 gene.

This genetic test can be useful in diagnosing LQT5 and determining the specific mutation present in an individual. It can also be used for carrier testing in family members of affected individuals and for prenatal testing in families with a known KCNE1 gene mutation.

It is important to note that genetic testing for LQT5 should be performed and interpreted by a qualified healthcare professional, such as a genetic counselor or a medical geneticist, who can provide appropriate counseling and guidance based on the test results.

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