Cardiomyopathy is a group of diseases that affect the heart muscle, leading to decreased heart function and an array of associated health issues. Among these, Familial Restrictive Cardiomyopathy (FRC) is a less common type characterized by the heart becoming too stiff to fill properly with blood. One of the genetic markers associated with this condition is mutations in the TNNI3 gene. DNA Labs UAE offers a comprehensive genetic test for this condition, providing crucial information for affected individuals and their families.
Symptoms of TNNI3 Gene Cardiomyopathy Familial Restrictive Type 1
Familial Restrictive Cardiomyopathy (FRC) caused by mutations in the TNNI3 gene can lead to a range of symptoms, often making it difficult to diagnose without genetic testing. The symptoms can vary widely among affected individuals, even within the same family, but typically include:
- Shortness of breath: This is often noticed during physical activity but can also occur at rest in more severe cases.
- Swelling: Accumulation of fluid can lead to swelling in the legs, ankles, and abdomen.
- Heart palpitations: Irregular heartbeats or feelings of the heart racing can be a common symptom.
- Fatigue: Affected individuals may experience unusual tiredness or weakness, making daily activities challenging.
- Chest pain: This can occur during physical activity or stress.
It’s important to note that these symptoms can be indicative of various heart conditions, making the genetic test for TNNI3 gene mutations a critical tool for accurate diagnosis.
Genetic Test for TNNI3 Gene Cardiomyopathy Familial Restrictive Type 1
DNA Labs UAE offers a genetic test specifically designed to detect mutations in the TNNI3 gene associated with Familial Restrictive Cardiomyopathy. This test is crucial for individuals who have symptoms of cardiomyopathy or have a family history of the condition. By identifying the genetic cause, healthcare providers can better understand the condition, predict its progression, and tailor treatment plans to manage symptoms effectively.
The test involves a simple blood draw or cheek swab, depending on the method used by the lab. Once the sample is collected, it is analyzed for specific mutations in the TNNI3 gene that are known to cause Familial Restrictive Cardiomyopathy. The results of this test can help in making informed decisions about treatment and management, as well as providing valuable information for family planning.
Cost of the Genetic Test
The cost of the TNNI3 Gene Cardiomyopathy Familial Restrictive Type 1 Genetic Test at DNA Labs UAE is 4400 AED. This cost includes the collection of the sample, analysis, and a comprehensive report of the findings. It’s important for potential patients to consult with their healthcare provider to understand the full scope of the test’s benefits and to discuss any questions they may have about the process or the implications of the results.
Conclusion
Familial Restrictive Cardiomyopathy is a serious condition that can significantly impact the quality of life. Early detection and diagnosis through genetic testing can provide affected individuals and their families with crucial information for managing the condition. DNA Labs UAE’s genetic test for TNNI3 gene mutations is a valuable resource for those seeking answers and a path forward in the management of Familial Restrictive Cardiomyopathy. For more information or to schedule a test, visit DNA Labs UAE.
