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ACTC1 Gene Cardiomyopathy dilated type 1R Genetic Test

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

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The “ACTC1 Gene Cardiomyopathy Dilated Type 1R Genetic Test” is a specialized diagnostic procedure offered at DNA Labs UAE, designed to identify mutations in the ACTC1 gene that are associated with Dilated Cardiomyopathy Type 1R (DCM1R). Dilated cardiomyopathy is a condition characterized by the enlargement and weakening of the heart’s main pumping chamber, which can lead to heart failure and other complications. The ACTC1 gene plays a crucial role in the structure and function of heart muscle cells, and mutations in this gene can disrupt heart muscle function, leading to DCM1R.

This genetic test involves collecting a DNA sample, typically through a blood draw or a cheek swab, and analyzing the genetic material for specific mutations in the ACTC1 gene. It is a powerful tool for early diagnosis, allowing for timely intervention and personalized treatment plans to manage symptoms and improve the quality of life for affected individuals.

The cost of the ACTC1 Gene Cardiomyopathy Dilated Type 1R Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the specialized nature of the test, including the sophisticated technology and expertise required to accurately identify mutations in the ACTC1 gene. Early diagnosis through this genetic test can be crucial for individuals with a family history of dilated cardiomyopathy, as it provides valuable information for managing the condition and reducing the risk of complications.

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ACTC1 Gene Cardiomyopathy dilated type 1R Genetic Test

At DNA Labs UAE, we offer the ACTC1 Gene Cardiomyopathy dilated type 1R Genetic Test at a cost of 4400.0 AED. This test is used to diagnose individuals with dilated cardiomyopathy type 1R (CMD1R), a condition characterized by an enlarged and weakened heart muscle.

Test Components

  • Price: 4400.0 AED
  • Sample Condition: Blood
  • Report Delivery: 3 to 4 Weeks
  • Method: NGS Technology
  • Test Type: Cardiovascular Pneumology Disorders
  • Doctor: Cardiologist
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the ACTC1 Gene Cardiomyopathy dilated type 1R Genetic Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with ACTC1 Gene Cardiomyopathy, dilated type 1R NGS Genetic DNA Test gene ACTC1.

Test Details

The ACTC1 gene is responsible for encoding a protein called cardiac alpha-actin, which is primarily found in the heart muscle. Mutations in the ACTC1 gene have been associated with dilated cardiomyopathy type 1R (CMD1R). CMD1R is an inherited form of dilated cardiomyopathy.

NGS (Next-Generation Sequencing) genetic testing is used to analyze multiple genes simultaneously, including the ACTC1 gene, to detect mutations associated with cardiomyopathies. This test helps in diagnosing individuals with CMD1R and identifying at-risk family members.

NGS genetic testing provides valuable information for the management and treatment of individuals with CMD1R. It also aids in genetic counseling, allowing for early detection and intervention in at-risk individuals.

Test Name ACTC1 Gene Cardiomyopathy dilated type 1R Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood
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 ACTC1 Gene Cardiomyopathy, dilated type 1R NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ACTC1 Gene Cardiomyopathy, dilated type 1R NGS Genetic DNA Test gene ACTC1
Test Details

The ACTC1 gene is responsible for encoding a protein called cardiac alpha-actin, which is primarily found in the heart muscle. Mutations in the ACTC1 gene have been associated with a type of cardiomyopathy called dilated cardiomyopathy type 1R (CMD1R).

Dilated cardiomyopathy (DCM) is a condition characterized by an enlarged and weakened heart muscle, leading to reduced pumping efficiency. CMD1R is an inherited form of DCM, meaning it is passed down through families.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, allowing for the detection of mutations in the ACTC1 gene and other genes associated with cardiomyopathies. This type of genetic testing can help in diagnosing individuals with CMD1R and identifying family members who may be at risk of developing the condition.

By identifying mutations in the ACTC1 gene, NGS genetic testing can provide valuable information for the management and treatment of individuals with CMD1R. It can also help in genetic counseling, allowing for early detection and intervention in at-risk individuals.

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