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TNNT2 Gene Cardiomyopathy Dilated Type 1D Genetic Test

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

-21%

The TNNT2 gene plays a crucial role in the structure and function of the heart muscle, and mutations in this gene are associated with dilated cardiomyopathy type 1D (DCM1D), a condition characterized by the enlargement and weakening of the heart’s left ventricle, leading to reduced heart function. The TNNT2 Gene Cardiomyopathy Dilated Type 1D Genetic Test is a specialized diagnostic tool designed to identify mutations in the TNNT2 gene, providing crucial information for the diagnosis, treatment planning, and familial risk assessment of DCM1D.

Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, this test is a critical resource for individuals with a family history of dilated cardiomyopathy or those exhibiting symptoms of the condition. The test cost is 4400 AED, reflecting the comprehensive analysis and the sophisticated technology employed to accurately detect the specific genetic alterations within the TNNT2 gene. By opting for this test, patients and healthcare providers can gain valuable insights into the genetic underpinnings of dilated cardiomyopathy, enabling informed decisions regarding management and therapy options, as well as the potential need for family member testing to assess inherited risks.

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TNNT2 Gene Cardiomyopathy Dilated Type 1D Genetic Test

Test Name: TNNT2 Gene Cardiomyopathy Dilated Type 1D Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

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 TNNT2 Gene Cardiomyopathy, dilated type 1D NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TNNT2 Gene Cardiomyopathy, dilated type 1D NGS Genetic DNA Test gene TNNT2

Test Details

TNNT2 gene cardiomyopathy, dilated type 1D is a genetic condition that affects the heart muscle. It is characterized by the dilation and weakening of the heart, leading to decreased pumping ability and potentially causing heart failure.

NGS (Next-Generation Sequencing) genetic testing is a diagnostic test used to identify genetic mutations in an individual’s DNA. In the case of TNNT2 gene cardiomyopathy, dilated type 1D, NGS genetic testing can be used to analyze the TNNT2 gene for any mutations or variations that may be associated with the condition.

The TNNT2 gene provides instructions for making a protein called cardiac troponin T, which is involved in the regulation of muscle contraction in the heart. Mutations in the TNNT2 gene can disrupt the normal function of cardiac troponin T, leading to the development of cardiomyopathy.

NGS genetic testing for TNNT2 gene cardiomyopathy, dilated type 1D involves obtaining a DNA sample, typically through a blood sample or cheek swab. The DNA is then sequenced using advanced sequencing technologies, allowing for the detection of any mutations or variations in the TNNT2 gene.

The results of the NGS genetic test can help diagnose TNNT2 gene cardiomyopathy, dilated type 1D in individuals with symptoms or a family history of the condition. It can also be used for carrier testing in individuals with a family history of the condition but no symptoms.

Genetic testing can provide valuable information for individuals and their families, including guidance for medical management, family planning, and genetic counseling. It is important to consult with a healthcare professional or genetic counselor to understand the implications of the test results and to discuss any further steps or recommendations.

Test Name TNNT2 Gene Cardiomyopathy dilated type 1D 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 TNNT2 Gene Cardiomyopathy, dilated type 1D NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TNNT2 Gene Cardiomyopathy, dilated type 1D NGS Genetic DNA Test gene TNNT2
Test Details

TNNT2 gene cardiomyopathy, dilated type 1D is a genetic condition that affects the heart muscle. It is characterized by the dilation and weakening of the heart, leading to decreased pumping ability and potentially causing heart failure.

NGS (Next-Generation Sequencing) genetic testing is a diagnostic test used to identify genetic mutations in an individual’s DNA. In the case of TNNT2 gene cardiomyopathy, dilated type 1D, NGS genetic testing can be used to analyze the TNNT2 gene for any mutations or variations that may be associated with the condition.

The TNNT2 gene provides instructions for making a protein called cardiac troponin T, which is involved in the regulation of muscle contraction in the heart. Mutations in the TNNT2 gene can disrupt the normal function of cardiac troponin T, leading to the development of cardiomyopathy.

NGS genetic testing for TNNT2 gene cardiomyopathy, dilated type 1D involves obtaining a DNA sample, typically through a blood sample or cheek swab. The DNA is then sequenced using advanced sequencing technologies, allowing for the detection of any mutations or variations in the TNNT2 gene.

The results of the NGS genetic test can help diagnose TNNT2 gene cardiomyopathy, dilated type 1D in individuals with symptoms or a family history of the condition. It can also be used for carrier testing in individuals with a family history of the condition but no symptoms.

Genetic testing can provide valuable information for individuals and their families, including guidance for medical management, family planning, and genetic counseling. It is important to consult with a healthcare professional or genetic counselor to understand the implications of the test results and to discuss any further steps or recommendations.

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