Short Description

NGS genetic DNA test detecets for variant and mutation detection in CSRP3 gene for Cardiomyopathy, dilated type 1M

PreTest Information

Clinical History of Patient who is going for CSRP3 Gene Cardiomyopathy, dilated type 1M NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CSRP3 Gene Cardiomyopathy, dilated type 1M NGS Genetic DNA Test gene CSRP3

Detail Description

CSRP3 Gene Cardiomyopathy, Dilated Type 1M: Symptoms, Diagnosis, and NGS Genetic DNA Test Cost

Cardiomyopathy is a disease that affects the heart muscle, making it harder for the heart to pump blood to the rest of the body. One type of cardiomyopathy is dilated cardiomyopathy, which occurs when the heart becomes enlarged and weakened. This condition can be caused by genetic mutations, and one such mutation is found in the CSRP3 gene. Here's what you need to know about CSRP3 gene cardiomyopathy, dilated type 1M, including its symptoms, diagnosis, and the cost of NGS genetic DNA testing.

Symptoms of CSRP3 Gene Cardiomyopathy, Dilated Type 1M

The symptoms of CSRP3 gene cardiomyopathy, dilated type 1M, can vary from person to person. Some people may have no symptoms at all, while others may experience:

• Shortness of breath
• Fatigue
• Swelling in the legs, ankles, or feet
• Irregular heartbeat
• Chest pain

These symptoms can develop gradually over time, and may worsen as the condition progresses.

Diagnosis of CSRP3 Gene Cardiomyopathy, Dilated Type 1M

If you're experiencing any of the symptoms listed above, your doctor may recommend that you undergo testing to determine if you have CSRP3 gene cardiomyopathy, dilated type 1M. The first step in diagnosis is typically a physical exam, during which your doctor will listen to your heart and lungs, check your blood pressure, and ask about your symptoms.

If your doctor suspects that you have cardiomyopathy, they may recommend further testing, such as:

• An electrocardiogram (ECG) to check your heart's electrical activity
• An echocardiogram to evaluate the size and function of your heart
• A chest X-ray to look for any abnormalities in the heart and lungs
• A cardiac MRI to provide detailed images of the heart
• A genetic test to determine if you have the CSRP3 gene mutation

Genetic testing can confirm a diagnosis of CSRP3 gene cardiomyopathy, dilated type 1M, and can also help identify other family members who may be at risk for the condition.

NGS Genetic DNA Test Cost for CSRP3 Gene Cardiomyopathy, Dilated Type 1M

The cost of NGS genetic DNA testing for CSRP3 gene cardiomyopathy, dilated type 1M can vary depending on the laboratory that performs the test. On average, the cost of this test in India is around INR 20,000.

It's important to note that genetic testing is not always covered by insurance, so it's a good idea to check with your insurance provider before undergoing testing. Additionally, some laboratories may offer financial assistance or payment plans to help offset the cost of testing.

Conclusion

CSRP3 gene cardiomyopathy, dilated type 1M is a genetic condition that can cause the heart to become enlarged and weakened. Symptoms may include shortness of breath, fatigue, swelling, irregular heartbeat, and chest pain. A variety of tests, including genetic testing, can be used to diagnose this condition. The cost of NGS genetic DNA testing for CSRP3 gene cardiomyopathy, dilated type 1M is around INR 20,000, but may vary depending on the laboratory and insurance coverage. If you're experiencing symptoms of cardiomyopathy, it's important to speak with your doctor to determine the best course of action.