Short Description

NGS genetic DNA test detecets for variant and mutation detection in MYL2 gene for Cardiomyopathy, familial hypertrophic type 10

PreTest 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

Detail Description

MYL2 Gene Cardiomyopathy: Symptoms, Diagnosis and NGS Genetic DNA Test Cost in India

Cardiomyopathy is a heart disease that affects the muscles of the heart, making it harder for the heart to pump blood effectively. Familial hypertrophic cardiomyopathy (FHC) is a type of cardiomyopathy that is inherited and affects the heart's muscle cells. MYL2 gene cardiomyopathy is a specific type of FHC that is caused by a mutation in the MYL2 gene. In this blog, we will discuss the symptoms, diagnosis, and NGS genetic DNA test cost for MYL2 gene cardiomyopathy in India.

Symptoms of MYL2 Gene Cardiomyopathy

The symptoms of MYL2 gene cardiomyopathy can vary from person to person. Some people may have no symptoms at all, while others may experience severe symptoms. The most common symptoms of MYL2 gene cardiomyopathy include:

• Chest pain or discomfort
• Shortness of breath
• Fainting or dizziness
• Heart palpitations
• Swelling in the legs, ankles, or feet

If you experience any of these symptoms, it is important to see a doctor as soon as possible.

Diagnosis of MYL2 Gene Cardiomyopathy

MYL2 gene cardiomyopathy is diagnosed through a series of tests. Your doctor will start by taking a detailed medical history and performing a physical exam. They may also order the following tests:

• Electrocardiogram (ECG)
• Echocardiogram
• Cardiac MRI
• Genetic testing

Genetic testing is particularly important for MYL2 gene cardiomyopathy as it can confirm the diagnosis and identify other family members who may be at risk for the disease.

NGS Genetic DNA Test Cost for MYL2 Gene Cardiomyopathy in India

The cost of NGS genetic DNA testing for MYL2 gene cardiomyopathy in India can vary depending on the laboratory and the specific tests ordered. However, on average, the cost of NGS genetic DNA testing for MYL2 gene cardiomyopathy in India is around INR 20,000.

Conclusion

MYL2 gene cardiomyopathy is a type of familial hypertrophic cardiomyopathy that is caused by a mutation in the MYL2 gene. The symptoms of MYL2 gene cardiomyopathy can vary, but may include chest pain, shortness of breath, and heart palpitations. If you experience any of these symptoms, it is important to see a doctor as soon as possible. MYL2 gene cardiomyopathy can be diagnosed through a series of tests, including genetic testing. The cost of NGS genetic DNA testing for MYL2 gene cardiomyopathy in India is around INR 20,000.

If you are concerned about your risk for MYL2 gene cardiomyopathy, talk to your doctor about genetic testing and other preventive measures.

Before getting tested ask for Raw Data, FASTQ, and VCF files along with clinical test report from DNA Testing Lab. DNA Labs India is the Only lab that is transparent and will share Raw Data, FASTQ, and VCF files along with the conclusive clinical report for MYL2 Gene Cardiomyopathy, familial hypertrophic type 10 NGS Genetic DNA Test