Short Description

NGS genetic DNA test detecets for variant and mutation detection in MYBPC3 gene for Cardiomyopathy, familial hypertrophic type 4

PreTest Information

Clinical History of Patient who is going for MYBPC3 Gene Cardiomyopathy, familial hypertrophic type 4 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MYBPC3 Gene Cardiomyopathy, familial hypertrophic type 4 NGS Genetic DNA Test gene MYBPC3

Detail Description

MYBPC3 Gene Cardiomyopathy: Symptoms, Diagnosis and NGS Genetic DNA Test Cost

Introduction

Cardiomyopathy is a heart disease that affects the structure and function of the heart muscles. Familial hypertrophic cardiomyopathy (FHC) is a type of cardiomyopathy that is inherited and affects the heart muscles, leading to thickening of the walls of the heart. FHC is caused by mutations in different genes, one of which is the MYBPC3 gene. In this blog, we will discuss MYBPC3 gene cardiomyopathy, its symptoms, diagnosis, and the NGS genetic DNA test cost in India.

Symptoms of MYBPC3 Gene Cardiomyopathy

The symptoms of MYBPC3 gene cardiomyopathy may vary from person to person and can range from mild to severe. Some of the common symptoms of MYBPC3 gene cardiomyopathy include:

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

It is important to note that not all people with MYBPC3 gene mutations will develop cardiomyopathy or experience symptoms.

Diagnosis of MYBPC3 Gene Cardiomyopathy

MYBPC3 gene cardiomyopathy can be diagnosed through a combination of medical history, physical examination, and diagnostic tests. Some of the diagnostic tests that may be used to diagnose MYBPC3 gene cardiomyopathy include:

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

Genetic testing is an important tool in the diagnosis of MYBPC3 gene cardiomyopathy. It involves analyzing a person's DNA to look for mutations in the MYBPC3 gene. This test can help identify individuals who are at risk of developing the condition or those who may have already developed the condition.

NGS Genetic DNA Test Cost for MYBPC3 Gene Cardiomyopathy in India

The cost of NGS genetic DNA test for MYBPC3 gene cardiomyopathy in India can vary depending on the laboratory and the location. On average, the cost of this test is around INR 20,000. It is important to note that this cost may not include the cost of consultation with a medical geneticist or genetic counselor.

Conclusion

MYBPC3 gene cardiomyopathy is a type of familial hypertrophic cardiomyopathy that is caused by mutations in the MYBPC3 gene. The symptoms of MYBPC3 gene cardiomyopathy may vary from person to person and can range from mild to severe. Diagnosis of MYBPC3 gene cardiomyopathy involves a combination of medical history, physical examination, and diagnostic tests, including genetic testing. The cost of NGS genetic DNA test for MYBPC3 gene cardiomyopathy in India can vary depending on the laboratory and the location. If you have any concerns or questions about MYBPC3 gene cardiomyopathy, it is important to consult with a medical geneticist or genetic counselor.

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 MYBPC3 Gene Cardiomyopathy, familial hypertrophic type 4 NGS Genetic DNA Test