ACTC1 Gene Cardiomyopathy familial hypertrophic type 11 Genetic Test sale cost 4400 AED
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ACTC1 Gene Cardiomyopathy familial hypertrophic type 11 Genetic Test Cost

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

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The ACTC1 gene plays a crucial role in the development and function of heart muscle. Mutations in this gene are associated with familial hypertrophic cardiomyopathy type 11 (HCM11), a genetic disorder characterized by the thickening of the heart’s ventricular walls. This condition can lead to various complications, including heart failure, arrhythmias, and sudden cardiac death.

To diagnose this condition, DNA Labs UAE offers a genetic test specifically targeting the ACTC1 gene. This test is designed to identify mutations within the gene that are linked to familial hypertrophic cardiomyopathy. Early detection through genetic testing is crucial for managing the condition, allowing for timely intervention and management strategies to mitigate the risk of complications.

The cost of the ACTC1 Gene Cardiomyopathy familial hypertrophic type 11 Genetic Test at DNA Labs UAE is 4400 AED. This test is a valuable resource for individuals with a family history of cardiomyopathy, providing them with critical information about their genetic predisposition to the condition. With this knowledge, affected individuals and their healthcare providers can make informed decisions regarding surveillance, lifestyle adjustments, and potential treatments to improve heart health and quality of life.

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ACTC1 Gene Cardiomyopathy Familial Hypertrophic Type 11 Genetic Test

Genetic testing plays a crucial role in diagnosing and understanding various genetic disorders. One such disorder is ACTC1 gene cardiomyopathy, familial hypertrophic type 11. This specific genetic disorder affects the heart muscle and is caused by mutations in the ACTC1 gene.

Test Details

The ACTC1 Gene Cardiomyopathy Familial Hypertrophic Type 11 Genetic Test is available at DNA Labs UAE. This test utilizes NGS (Next-Generation Sequencing) technology to analyze the DNA sequence of the ACTC1 gene. The test helps identify any mutations or variations in the gene that may be associated with the condition. The test components include:

  • Test Name: ACTC1 Gene Cardiomyopathy Familial Hypertrophic Type 11 Genetic Test
  • 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

Symptoms and Diagnosis

Familial hypertrophic cardiomyopathy (FHC) refers to a group of diseases that affect the structure and function of the heart muscle. In the case of ACTC1 gene cardiomyopathy, familial hypertrophic type 11, the heart muscle becomes abnormally thickened, making it harder for the heart to pump blood effectively. Symptoms of this condition may include:

  • Shortness of breath
  • Chest pain
  • Fatigue
  • Fainting or dizziness
  • Heart palpitations

Diagnosing ACTC1 gene cardiomyopathy, familial hypertrophic type 11 requires a genetic test, such as the ACTC1 Gene Cardiomyopathy Familial Hypertrophic Type 11 Genetic Test. It is important to consult with a healthcare professional or genetic counselor who can interpret the test results and provide appropriate recommendations.

Pre-Test Information

Before undergoing the ACTC1 Gene Cardiomyopathy Familial Hypertrophic Type 11 Genetic Test, it is recommended to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by the condition. This information helps in understanding the inheritance pattern and identifying potential carriers of the ACTC1 gene mutation.

Conclusion

The ACTC1 Gene Cardiomyopathy Familial Hypertrophic Type 11 Genetic Test offered by DNA Labs UAE is a valuable tool for diagnosing and understanding ACTC1 gene cardiomyopathy, familial hypertrophic type 11. It utilizes NGS technology to identify specific mutations in the ACTC1 gene that may be causing the condition. This information can assist in diagnosis, genetic counseling, and potentially guiding treatment decisions. It is essential to seek guidance from healthcare professionals or genetic counselors for the interpretation of test results and appropriate recommendations.

Test Name ACTC1 Gene Cardiomyopathy familial hypertrophic type 11 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, familial hypertrophic type 11 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ACTC1 Gene Cardiomyopathy, familial hypertrophic type 11 NGS Genetic DNA Test gene ACTC1
Test Details

ACTC1 gene cardiomyopathy, familial hypertrophic type 11 is a specific type of genetic disorder that affects the heart muscle. It is caused by mutations in the ACTC1 gene, which provides instructions for making a protein called cardiac alpha-actin.

Cardiomyopathy refers to a group of diseases that affect the structure and function of the heart muscle. In familial hypertrophic cardiomyopathy (FHC), the heart muscle becomes abnormally thickened, making it harder for the heart to pump blood effectively.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously. It uses advanced sequencing technology to examine the DNA sequence of specific genes, such as the ACTC1 gene, to identify any mutations or variations that may be associated with a particular condition.

In the case of ACTC1 gene cardiomyopathy, familial hypertrophic type 11, NGS genetic testing can help identify specific mutations in the ACTC1 gene that may be causing the condition. This information can be used for diagnosis, genetic counseling, and potentially guiding treatment decisions.

It’s important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor who can interpret the results and provide appropriate recommendations.

SKU: TEST-3397 Category:

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