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DSG2 Gene Cardiomyopathy Dilated Type 1BB Genetic Test Cost

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

-21%

The DSG2 Gene Cardiomyopathy Dilated Type 1BB Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the DSG2 gene, which have been associated with dilated cardiomyopathy (DCM) type 1BB. Dilated cardiomyopathy is a condition characterized by the enlargement and weakening of the heart’s main pumping chamber, leading to decreased heart function and, in severe cases, heart failure. The DSG2 gene plays a crucial role in the structure and function of heart muscle cells, and mutations in this gene can disrupt heart muscle function, contributing to the development of DCM.

This genetic test is particularly valuable for individuals with a family history of dilated cardiomyopathy or unexplained heart failure, as it can provide a definitive diagnosis of DCM type 1BB. Early detection through genetic testing allows for timely intervention and management of the condition, potentially improving outcomes for affected individuals.

The test is conducted at DNA Labs UAE, a facility known for its advanced genetic testing services. The cost of the DSG2 Gene Cardiomyopathy Dilated Type 1BB Genetic Test is 4400 AED, reflecting the sophisticated nature of the testing process and the specialized expertise required to interpret the results. This test is an important resource for individuals and families seeking clarity on their genetic risk for dilated cardiomyopathy, enabling them to make informed decisions about their health and care.

Description

DSG2 Gene Cardiomyopathy dilated type 1BB Genetic Test

Test Name: DSG2 Gene Cardiomyopathy dilated type 1BB Genetic Test

Components: NGS Technology

Price: 4400.0 AED

Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery: 3 to 4 Weeks

Test Type: Cardiovascular Pneumology Disorders

Doctor: Cardiologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for DSG2 Gene Cardiomyopathy, dilated type 1BB NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with DSG2 Gene Cardiomyopathy, dilated type 1BB NGS Genetic DNA Test gene DSG2

Test Details: DSG2 gene cardiomyopathy, dilated type 1BB is a type of genetic cardiomyopathy that is caused by mutations in the DSG2 gene. This gene provides instructions for making a protein called desmoglein-2, which is found in the heart muscle cells. Desmoglein-2 is a component of desmosomes, which are structures that help hold cells together. Mutations in the DSG2 gene can disrupt the normal function of desmoglein-2, leading to a weakening and stretching of the heart muscle (dilated cardiomyopathy). This can result in symptoms such as heart failure, arrhythmias, and an increased risk of sudden cardiac death.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously to identify mutations or variations that may be associated with a specific condition. In the case of DSG2 gene cardiomyopathy, NGS genetic testing can be used to identify mutations in the DSG2 gene that may be causing the condition.

NGS genetic testing for DSG2 gene cardiomyopathy, dilated type 1BB can help with the diagnosis of the condition, as well as provide information about the specific genetic mutation involved. This information can be useful for guiding treatment decisions, as well as for providing information to family members who may be at risk of inheriting the condition.

It is important to note that genetic testing for DSG2 gene cardiomyopathy, dilated type 1BB is typically performed by healthcare professionals, such as genetic counselors or geneticists, who can provide appropriate counseling and interpretation of the results.

Test Name	DSG2 Gene Cardiomyopathy dilated type 1BB 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 DSG2 Gene Cardiomyopathy, dilated type 1BB NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with DSG2 Gene Cardiomyopathy, dilated type 1BB NGS Genetic DNA Test gene DSG2
Test Details	DSG2 gene cardiomyopathy, dilated type 1BB is a type of genetic cardiomyopathy that is caused by mutations in the DSG2 gene. This gene provides instructions for making a protein called desmoglein-2, which is found in the heart muscle cells. Desmoglein-2 is a component of desmosomes, which are structures that help hold cells together. Mutations in the DSG2 gene can disrupt the normal function of desmoglein-2, leading to a weakening and stretching of the heart muscle (dilated cardiomyopathy). This can result in symptoms such as heart failure, arrhythmias, and an increased risk of sudden cardiac death. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously to identify mutations or variations that may be associated with a specific condition. In the case of DSG2 gene cardiomyopathy, NGS genetic testing can be used to identify mutations in the DSG2 gene that may be causing the condition. NGS genetic testing for DSG2 gene cardiomyopathy, dilated type 1BB can help with the diagnosis of the condition, as well as provide information about the specific genetic mutation involved. This information can be useful for guiding treatment decisions, as well as for providing information to family members who may be at risk of inheriting the condition. It is important to note that genetic testing for DSG2 gene cardiomyopathy, dilated type 1BB is typically performed by healthcare professionals, such as genetic counselors or geneticists, who can provide appropriate counseling and interpretation of the results.