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SCN4B Gene Long QT syndrome type 10 Genetic Test

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

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The SCN4B gene plays a critical role in cardiac electrophysiology, and mutations in this gene are associated with Long QT Syndrome Type 10 (LQT10), a rare inherited heart condition. This condition can lead to irregular heartbeats, fainting, and even sudden death, especially under stress or during exercise. It’s crucial for individuals with a family history of Long QT Syndrome or unexplained cardiac events to undergo genetic testing to identify potential risks.

DNA Labs UAE offers a genetic test specifically targeting the SCN4B gene to diagnose Long QT Syndrome Type 10. This test is pivotal for individuals suspecting they might carry this mutation, providing them with crucial information about their heart health and the necessary precautions to take. The test cost is 4400 AED, a valuable investment in personal health and well-being, especially for those at risk. Early detection through this test can lead to better management of the condition, including lifestyle adjustments and possibly medication to prevent life-threatening cardiac events.

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SCN4B Gene Long QT Syndrome Type 10 Genetic Test

Components: SCN4B Gene Long QT syndrome type 10 Genetic Test

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 SCN4B Gene Long QT syndrome type 10 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SCN4B Gene Long QT syndrome type 10 NGS Genetic DNA Test gene SCN4B

Test Details

The SCN4B gene is associated with Long QT syndrome type 10 (LQT10), also known as Brugada syndrome. LQT10 is a rare genetic disorder that affects the heart’s electrical system, leading to abnormal heart rhythms and an increased risk of sudden cardiac arrest.

NGS (Next-Generation Sequencing) genetic testing is a type of DNA sequencing technology that allows for the simultaneous analysis of multiple genes, including the SCN4B gene. This test can identify specific mutations or variations in the SCN4B gene that may be responsible for causing LQT10.

By detecting these genetic abnormalities, NGS testing can help diagnose individuals with Long QT syndrome type 10 and guide appropriate treatment and management strategies. It can also be used for genetic counseling and family screening to identify individuals at risk of inheriting the condition.

It is important to note that NGS testing for Long QT syndrome type 10 should be performed by a qualified genetic testing laboratory or healthcare provider with expertise in genetic testing and cardiovascular disorders. The results of the test should be interpreted by a medical professional trained in genetics and cardiology to ensure accurate diagnosis and appropriate management.

Test Name SCN4B Gene Long QT syndrome type 10 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 SCN4B Gene Long QT syndrome type 10 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SCN4B Gene Long QT syndrome type 10 NGS Genetic DNA Test gene SCN4B
Test Details

The SCN4B gene is associated with Long QT syndrome type 10 (LQT10), also known as Brugada syndrome. LQT10 is a rare genetic disorder that affects the heart’s electrical system, leading to abnormal heart rhythms and an increased risk of sudden cardiac arrest.

NGS (Next-Generation Sequencing) genetic testing is a type of DNA sequencing technology that allows for the simultaneous analysis of multiple genes, including the SCN4B gene. This test can identify specific mutations or variations in the SCN4B gene that may be responsible for causing LQT10.

By detecting these genetic abnormalities, NGS testing can help diagnose individuals with Long QT syndrome type 10 and guide appropriate treatment and management strategies. It can also be used for genetic counseling and family screening to identify individuals at risk of inheriting the condition.

It is important to note that NGS testing for Long QT syndrome type 10 should be performed by a qualified genetic testing laboratory or healthcare provider with expertise in genetic testing and cardiovascular disorders. The results of the test should be interpreted by a medical professional trained in genetics and cardiology to ensure accurate diagnosis and appropriate management.

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