Short Description

NGS genetic DNA test detecets for variant and mutation detection in PRKAG2 gene for Cardiomyopathy, familial hypertrophic type 6

PreTest Information

Clinical History of Patient who is going for PRKAG2 Gene Cardiomyopathy, familial hypertrophic type 6 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PRKAG2 Gene Cardiomyopathy, familial hypertrophic type 6 NGS Genetic DNA Test gene PRKAG2

Detail Description

PRKAG2 Gene Cardiomyopathy: Symptoms, Diagnosis and NGS Genetic DNA Test Cost in India

Cardiomyopathy is a group of diseases that affect the heart muscle. It causes the heart to become enlarged, thick, or stiff, which can lead to heart failure or other complications. Familial hypertrophic cardiomyopathy (FHC) is a type of cardiomyopathy that runs in families and is caused by mutations in certain genes.

One of the genes associated with FHC is the PRKAG2 gene. Mutations in this gene can cause familial hypertrophic cardiomyopathy type 6 (FHC6). This type of cardiomyopathy is rare, but it can be life-threatening if not diagnosed and treated early.

Symptoms of PRKAG2 Gene Cardiomyopathy

The symptoms of PRKAG2 gene cardiomyopathy can vary from person to person, even within the same family. Some people may have no symptoms at all, while others may have severe symptoms that can lead to heart failure or sudden death.

Common symptoms of PRKAG2 gene cardiomyopathy include:

• Chest pain or discomfort
• Shortness of breath, especially during exercise
• Fatigue
• Dizziness or fainting
• Irregular heartbeat

Diagnosis of PRKAG2 Gene Cardiomyopathy

If you have symptoms of PRKAG2 gene cardiomyopathy, your doctor may recommend several tests to diagnose the condition. These tests may include:

• Echocardiogram: This test uses sound waves to create images of your heart. It can show if your heart is enlarged or if the walls are thickened.
• Electrocardiogram (ECG): This test records the electrical activity of your heart. It can detect abnormal heart rhythms or other problems.
• Genetic testing: This test can detect mutations in the PRKAG2 gene that cause FHC6. It may be recommended if you have a family history of FHC or if other tests are inconclusive.

NGS Genetic DNA Test Cost for PRKAG2 Gene Cardiomyopathy in India

The cost of NGS genetic DNA testing for PRKAG2 gene cardiomyopathy in India is approximately INR 20,000. This test can detect mutations in the PRKAG2 gene that cause FHC6. It is a highly accurate test that can help diagnose the condition early and prevent complications.

If you have a family history of FHC or if you have symptoms of PRKAG2 gene cardiomyopathy, talk to your doctor about genetic testing. Early diagnosis and treatment can help improve your prognosis and prevent complications.

Conclusion

PRKAG2 gene cardiomyopathy is a rare form of familial hypertrophic cardiomyopathy that can be life-threatening if not diagnosed and treated early. If you have a family history of FHC or if you have symptoms of PRKAG2 gene cardiomyopathy, talk to your doctor about genetic testing. The NGS genetic DNA test for PRKAG2 gene cardiomyopathy in India costs approximately INR 20,000 and can help diagnose the condition early and prevent complications.

Remember, early detection is the key to managing cardiomyopathy and improving your quality of life. So, don't hesitate to talk to your doctor if you have concerns about your heart health.

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 PRKAG2 Gene Cardiomyopathy, familial hypertrophic type 6 NGS Genetic DNA Test