Short Description

NGS genetic DNA test detecets for variant and mutation detection in MYH7 gene for Cardiomyopathy, familial hypertrophic type 1

PreTest Information

Clinical History of Patient who is going for MYH7 Gene Cardiomyopathy, familial hypertrophic type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MYH7 Gene Cardiomyopathy, familial hypertrophic type 1 NGS Genetic DNA Test gene MYH7

Detail Description

MYH7 Gene Cardiomyopathy: Symptoms, Diagnosis and NGS Genetic DNA Test Cost

Cardiomyopathy is a heart disease that affects the heart muscles, making it difficult for the heart to pump blood to the rest of the body. There are various types of cardiomyopathy, including hypertrophic cardiomyopathy, which is a genetic condition that affects the heart muscles. MYH7 gene cardiomyopathy, familial hypertrophic type 1, is one of the most common genetic causes of hypertrophic cardiomyopathy.

Symptoms of MYH7 Gene Cardiomyopathy

The symptoms of MYH7 gene cardiomyopathy can vary from person to person. Some people may not experience any symptoms, while others may have severe symptoms. The common symptoms of MYH7 gene cardiomyopathy include:

• Chest pain
• Shortness of breath
• Fainting
• Heart palpitations
• Fatigue

These symptoms can be mild or severe and can appear at any age. However, the symptoms usually develop during adolescence or early adulthood.

Diagnosis of MYH7 Gene Cardiomyopathy

MYH7 gene cardiomyopathy is usually diagnosed through a combination of physical examination, medical history, and diagnostic tests. The doctor may perform a physical exam to check for any abnormal heart sounds or rhythms. They may also ask about the patient's medical history and family history of heart disease.

Diagnostic tests that may be performed to diagnose MYH7 gene cardiomyopathy include:

• Electrocardiogram (ECG)
• Echocardiogram
• Magnetic resonance imaging (MRI)
• Cardiac catheterization

Genetic testing may also be recommended to confirm the diagnosis of MYH7 gene cardiomyopathy. Genetic testing involves analyzing a blood or saliva sample to look for mutations in the MYH7 gene.

NGS Genetic DNA Test Cost for MYH7 Gene Cardiomyopathy

NGS (Next-Generation Sequencing) genetic DNA testing is a modern technique used to identify genetic mutations associated with various diseases, including MYH7 gene cardiomyopathy. NGS testing can detect genetic mutations in a more efficient and cost-effective way compared to traditional genetic testing methods.

The cost of NGS genetic DNA testing for MYH7 gene cardiomyopathy in India is around INR 20,000. The cost may vary depending on the laboratory and the location.

Conclusion

MYH7 gene cardiomyopathy is a genetic condition that affects the heart muscles and can cause various symptoms, including chest pain, shortness of breath, and fainting. The diagnosis of MYH7 gene cardiomyopathy involves a combination of physical examination, medical history, and diagnostic tests, including NGS genetic DNA testing. The cost of NGS genetic DNA testing for MYH7 gene cardiomyopathy in India is around INR 20,000. If you experience any symptoms of MYH7 gene cardiomyopathy, it is important to consult a doctor for diagnosis and treatment.

At DNA Labs India, we offer NGS genetic DNA testing for MYH7 gene cardiomyopathy to help patients identify the genetic mutations associated with the disease and receive appropriate treatment. Contact us today to schedule a consultation.

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 MYH7 Gene Cardiomyopathy, familial hypertrophic type 1 NGS Genetic DNA Test