Short Description

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

PreTest Information

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

Detail Description

DES Gene Cardiomyopathy, Dilated Type 1I NGS Genetic DNA Test: Symptoms, Diagnosis, and Cost in India

Cardiomyopathy is a heart disease that affects the heart muscle, making it harder for the heart to pump blood to the body. Dilated cardiomyopathy (DCM) is a type of cardiomyopathy that affects the heart's left ventricle and leads to an enlarged and weakened heart. DES gene cardiomyopathy, dilated type 1I is a rare form of dilated cardiomyopathy caused by a mutation in the DES gene. This genetic mutation affects the heart's ability to contract and relax properly, leading to heart failure.

Symptoms of DES Gene Cardiomyopathy

The symptoms of DES gene cardiomyopathy are similar to those of other types of dilated cardiomyopathy. Some of the common symptoms include:

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

These symptoms can vary in severity and may worsen over time. If you experience any of these symptoms, it is important to see a doctor for proper diagnosis and treatment.

Diagnosis of DES Gene Cardiomyopathy

Diagnosing DES gene cardiomyopathy can be challenging because it is a rare form of dilated cardiomyopathy. However, there are several tests that can help diagnose this condition, including:

• Electrocardiogram (ECG): This test measures the electrical activity of the heart and can detect irregular heart rhythms and other abnormalities.
• Echocardiogram: This test uses sound waves to create images of the heart and can detect an enlarged and weakened heart.
• Cardiac MRI: This test uses magnetic fields and radio waves to create detailed images of the heart and can detect abnormalities in the heart muscle.
• Genetic testing: This test can detect mutations in the DES gene that cause DES gene cardiomyopathy.

If you have a family history of dilated cardiomyopathy or have symptoms of heart failure, your doctor may recommend these tests to diagnose DES gene cardiomyopathy.

NGS Genetic DNA Test for DES Gene Cardiomyopathy

Next-generation sequencing (NGS) genetic DNA testing is a type of genetic testing that can detect mutations in the DES gene that cause DES gene cardiomyopathy. This test uses advanced technology to analyze your DNA and can detect even small mutations that may be missed by other genetic tests.

The cost of NGS genetic DNA testing for DES gene cardiomyopathy in India can vary depending on the provider and the specific test being performed. On average, the cost of this test is around INR 20,000.

Conclusion

DES gene cardiomyopathy, dilated type 1I is a rare form of dilated cardiomyopathy caused by a mutation in the DES gene. If you experience symptoms of heart failure or have a family history of dilated cardiomyopathy, it is important to see a doctor for proper diagnosis and treatment. NGS genetic DNA testing can help detect mutations in the DES gene that cause DES gene cardiomyopathy and can be performed at a cost of around INR 20,000 in India.

The DES gene is associated with a genetic condition known as "Dilated Cardiomyopathy, Type 1I" (also referred to as "Dilated Cardiomyopathy with Desmin-related Myopathy"). Dilated cardiomyopathy (DCM) is a heart disorder characterized by the enlargement and weakened function of the heart's main pumping chamber, the left ventricle. Mutations or variations in the DES gene can contribute to the development of this specific subtype of dilated cardiomyopathy.