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SCN3B Gene Brugada Syndrome Type 7 Genetic Test Cost

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

-21%

The SCN3B Gene Brugada Syndrome Type 7 Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the SCN3B gene that are associated with Brugada Syndrome Type 7. Brugada Syndrome is a potentially life-threatening heart condition that can cause dangerous irregular heart rhythms. These arrhythmias can lead to sudden cardiac arrest in otherwise healthy individuals, often without warning.

The test targets the SCN3B gene, which plays a crucial role in the proper function of heart cells. Mutations in this gene can disrupt the normal electrical activity of the heart, leading to the characteristic patterns observed in Brugada Syndrome. By detecting these specific genetic variations, the test can help in diagnosing individuals at risk of this condition, allowing for appropriate management strategies to be implemented.

Offered at a cost of 4400 AED, the SCN3B Gene Brugada Syndrome Type 7 Genetic Test at DNA Labs UAE represents a critical step forward in the early detection and prevention of sudden cardiac death associated with Brugada Syndrome. This test is particularly important for individuals with a family history of the condition or those who have experienced unexplained syncope or cardiac arrest, as it can provide vital information for risk assessment and treatment planning.

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SCN3B Gene Brugada Syndrome Type 7 Genetic Test

Cost: AED 4400.0

Test Components: SCN3B Gene Brugada syndrome type 7 Genetic Test

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 SCN3B Gene Brugada syndrome type 7 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SCN3B Gene Brugada syndrome type 7 NGS Genetic DNA Test gene SCN3B

Test Details

The SCN3B gene is a gene that codes for a subunit of the sodium channel in the heart. Variations or mutations in this gene can lead to a condition called Brugada syndrome, specifically type 7. Brugada syndrome is a genetic disorder that affects the electrical system of the heart, leading to an increased risk of abnormal heart rhythms and sudden cardiac death. It is characterized by specific electrocardiogram (ECG) patterns, including ST segment elevation in the right precordial leads.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes. In the context of Brugada syndrome, NGS testing can be used to analyze the SCN3B gene, along with other genes known to be associated with the condition, to identify any variations or mutations that may be present. NGS genetic testing can help confirm a diagnosis of Brugada syndrome and provide information about the specific genetic variant(s) involved. This information can be useful for making treatment decisions, assessing the risk of sudden cardiac death, and providing genetic counseling to affected individuals and their families.

Test Name SCN3B Gene Brugada syndrome type 7 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 SCN3B Gene Brugada syndrome type 7 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SCN3B Gene Brugada syndrome type 7 NGS Genetic DNA Test gene SCN3B
Test Details

The SCN3B gene is a gene that codes for a subunit of the sodium channel in the heart. Variations or mutations in this gene can lead to a condition called Brugada syndrome, specifically type 7.

Brugada syndrome is a genetic disorder that affects the electrical system of the heart, leading to an increased risk of abnormal heart rhythms and sudden cardiac death. It is characterized by specific electrocardiogram (ECG) patterns, including ST segment elevation in the right precordial leads.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes. In the context of Brugada syndrome, NGS testing can be used to analyze the SCN3B gene, along with other genes known to be associated with the condition, to identify any variations or mutations that may be present.

NGS genetic testing can help confirm a diagnosis of Brugada syndrome and provide information about the specific genetic variant(s) involved. This information can be useful for making treatment decisions, assessing the risk of sudden cardiac death, and providing genetic counseling to affected individuals and their families.

SKU: TEST-3342 Category:

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