MYL2 Gene Cardiomyopathy familial hypertrophic type 10 Genetic Test sale cost 4400 AED
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MYL2 Gene Cardiomyopathy familial hypertrophic type 10 Genetic Test Cost

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

-21%

The MYL2 gene is associated with a form of cardiomyopathy known as familial hypertrophic cardiomyopathy type 10 (HCM 10). This condition is characterized by the thickening of the heart muscle, which can lead to various complications, including heart failure, arrhythmias, and sudden cardiac death. The MYL2 gene encodes for the regulatory light chain of myosin, a protein essential for heart muscle contraction. Mutations in the MYL2 gene disrupt this process, leading to the development of HCM.

In the United Arab Emirates, DNA Labs UAE offers a genetic test specifically designed to identify mutations in the MYL2 gene associated with familial hypertrophic cardiomyopathy type 10. This test is crucial for individuals with a family history of HCM or those exhibiting symptoms related to heart muscle dysfunction, as it can confirm the diagnosis and facilitate appropriate management and treatment strategies.

The cost of the MYL2 Gene Cardiomyopathy Familial Hypertrophic Type 10 Genetic Test at DNA Labs UAE is 4400 AED. The test involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the laboratory to detect the presence of any genetic alterations in the MYL2 gene. The results of this test can provide valuable information for affected individuals and their families, including the risk of developing HCM, implications for family planning, and the need for regular cardiac monitoring or intervention.

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MYL2 Gene Cardiomyopathy familial hypertrophic type 10 Genetic Test

Test Name: MYL2 Gene Cardiomyopathy familial hypertrophic type 10 Genetic Test

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

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 MYL2 Gene Cardiomyopathy, familial hypertrophic type 10 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MYL2 Gene Cardiomyopathy, familial hypertrophic type 10 NGS Genetic DNA Test gene MYL2

Test Details: The MYL2 gene is associated with familial hypertrophic cardiomyopathy, which is a genetic condition characterized by the thickening of the heart muscle. This condition can lead to various cardiac problems, including heart failure, arrhythmias, and sudden cardiac death. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously and identify genetic variations or mutations associated with certain diseases or conditions. In the case of familial hypertrophic cardiomyopathy, NGS testing can help identify specific mutations in the MYL2 gene that may be responsible for the development of the condition. By performing this genetic test, healthcare providers can provide a more accurate diagnosis, assess the risk of developing cardiomyopathy in family members, and guide appropriate treatment and management strategies. Genetic counseling is often recommended before and after genetic testing to discuss the implications of the test results and help individuals and families make informed decisions regarding their healthcare.

Test Name MYL2 Gene Cardiomyopathy familial hypertrophic type 10 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 MYL2 Gene Cardiomyopathy, familial hypertrophic type 10 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MYL2 Gene Cardiomyopathy, familial hypertrophic type 10 NGS Genetic DNA Test gene MYL2
Test Details

The MYL2 gene is associated with familial hypertrophic cardiomyopathy, which is a genetic condition characterized by the thickening of the heart muscle. This condition can lead to various cardiac problems, including heart failure, arrhythmias, and sudden cardiac death.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously and identify genetic variations or mutations associated with certain diseases or conditions. In the case of familial hypertrophic cardiomyopathy, NGS testing can help identify specific mutations in the MYL2 gene that may be responsible for the development of the condition.

By performing this genetic test, healthcare providers can provide a more accurate diagnosis, assess the risk of developing cardiomyopathy in family members, and guide appropriate treatment and management strategies. Genetic counseling is often recommended before and after genetic testing to discuss the implications of the test results and help individuals and families make informed decisions regarding their healthcare.

SKU: TEST-3396 Category:

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