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BAG3 Gene Cardiomyopathy Dilated Type 1HH Genetic Test

4,400 د.إ

-21%

The “BAG3 Gene Cardiomyopathy Dilated Type 1HH Genetic Test” is a specialized diagnostic procedure offered by DNA Labs UAE, designed to detect mutations in the BAG3 gene, which are linked to Dilated Cardiomyopathy (DCM) type 1HH. Dilated Cardiomyopathy is a condition characterized by the heart’s diminished ability to pump blood due to an enlarged and weakened left ventricle. The BAG3 gene plays a crucial role in cardiac function and structure, and mutations in this gene can lead to early-onset DCM, often resulting in severe cardiac issues or heart failure.

This genetic test is critical for individuals with a family history of DCM or symptoms suggestive of the condition, as it can provide definitive diagnosis and guide treatment decisions. The test involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the lab to identify any genetic alterations in the BAG3 gene.

The cost of the test is 4400 AED, reflecting the specialized nature of the genetic analysis and the comprehensive insights it offers into the patient’s condition. By identifying BAG3 gene mutations, healthcare providers can better understand the disease’s progression, enabling more personalized and effective treatment plans, and potentially guiding family planning decisions for affected individuals or their relatives.

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BAG3 Gene Cardiomyopathy dilated type 1HH Genetic Test

Cost: AED 4400.0

Symptoms and Diagnosis

BAG3 gene cardiomyopathy, dilated type 1HH is a genetic disorder characterized by the weakening and enlargement of the heart muscle, leading to heart failure. It is caused by mutations in the BAG3 gene, which provides instructions for producing a protein involved in cell maintenance and regulation.

Test Components

  • 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 BAG3 Gene Cardiomyopathy, dilated type 1HH NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with BAG3 Gene Cardiomyopathy, dilated type 1HH NGS Genetic DNA Test gene BAG3.

Test Details

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze an individual’s DNA sequence for specific genetic mutations or variations. In the case of BAG3 gene cardiomyopathy, NGS genetic testing can identify mutations in the BAG3 gene that are responsible for the development of the condition. NGS genetic testing involves sequencing the entire or specific regions of an individual’s genome to detect variations in the DNA sequence. This allows for a comprehensive analysis of multiple genes simultaneously, providing a more efficient and accurate diagnosis compared to traditional sequencing methods.

By identifying the specific genetic mutation causing BAG3 gene cardiomyopathy, NGS genetic testing can help in the diagnosis, prognosis, and treatment planning for affected individuals. It can also be used for genetic counseling and family planning purposes, as it can determine the likelihood of passing on the condition to future generations.

Test Name BAG3 Gene Cardiomyopathy dilated type 1HH 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 BAG3 Gene Cardiomyopathy, dilated type 1HH NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with BAG3 Gene Cardiomyopathy, dilated type 1HH NGS Genetic DNA Test gene BAG3
Test Details

BAG3 gene cardiomyopathy, dilated type 1HH is a genetic disorder characterized by the weakening and enlargement of the heart muscle, leading to heart failure. It is caused by mutations in the BAG3 gene, which provides instructions for producing a protein involved in cell maintenance and regulation.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze an individual’s DNA sequence for specific genetic mutations or variations. In the case of BAG3 gene cardiomyopathy, NGS genetic testing can identify mutations in the BAG3 gene that are responsible for the development of the condition.

NGS genetic testing involves sequencing the entire or specific regions of an individual’s genome to detect variations in the DNA sequence. This allows for a comprehensive analysis of multiple genes simultaneously, providing a more efficient and accurate diagnosis compared to traditional sequencing methods.

By identifying the specific genetic mutation causing BAG3 gene cardiomyopathy, NGS genetic testing can help in the diagnosis, prognosis, and treatment planning for affected individuals. It can also be used for genetic counseling and family planning purposes, as it can determine the likelihood of passing on the condition to future generations.