Short Description

NGS genetic DNA test detecets for variant and mutation detection in JPH2 gene for Cardiomyopathy, familial hypertrophic type 17

PreTest Information

Clinical History of Patient who is going for JPH2 Gene Cardiomyopathy, familial hypertrophic type 17 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with JPH2 Gene Cardiomyopathy, familial hypertrophic type 17 NGS Genetic DNA Test gene JPH2

Detail Description

JPH2 Gene Cardiomyopathy: Symptoms, Diagnosis, and NGS Genetic DNA Test Cost in India

Cardiomyopathy is a genetic condition that affects the heart muscles and makes it harder for the heart to pump blood to the rest of the body. Familial hypertrophic cardiomyopathy (FHC) is a type of cardiomyopathy that is inherited and affects the heart's thickening muscles. JPH2 gene cardiomyopathy, familial hypertrophic type 17 is a specific type of FHC that is caused by mutations in the JPH2 gene.

Symptoms of JPH2 Gene Cardiomyopathy

The symptoms of JPH2 gene cardiomyopathy can vary from person to person, and some people may not have any symptoms at all. Common symptoms of JPH2 gene cardiomyopathy include:

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

It's important to note that many of these symptoms can also be signs of other heart conditions, so it's important to see a doctor for proper diagnosis.

Diagnosing JPH2 Gene Cardiomyopathy

Diagnosing JPH2 gene cardiomyopathy usually involves a combination of medical history, physical exam, and diagnostic tests. Your doctor may ask you about your family history of heart disease and any symptoms you are experiencing. They will also listen to your heart and lungs and may order one or more of the following tests:

• Electrocardiogram (ECG)
• Echocardiogram
• Magnetic resonance imaging (MRI)
• Genetic testing

Genetic testing is the most definitive way to diagnose JPH2 gene cardiomyopathy. A simple blood test can detect mutations in the JPH2 gene that are associated with this condition.

NGS Genetic DNA Test Cost in India

The cost of an NGS genetic DNA test for JPH2 gene cardiomyopathy in India can vary depending on the laboratory and the type of test being performed. However, on average, the cost of an NGS genetic DNA test for JPH2 gene cardiomyopathy is around INR 20,000.

Conclusion

JPH2 gene cardiomyopathy, familial hypertrophic type 17 is a serious genetic condition that can cause a range of symptoms and complications. If you or a family member have a history of heart disease or are experiencing symptoms like chest pain, shortness of breath, or palpitations, it's important to see a doctor for proper diagnosis. Genetic testing can help confirm a diagnosis of JPH2 gene cardiomyopathy and guide treatment decisions.

At DNA Labs India, we offer a range of genetic testing services, including NGS genetic DNA testing for JPH2 gene cardiomyopathy. Contact us today to learn more about our testing services and how we can help you get the answers you need.