Short Description

NGS genetic DNA test detecets for variant and mutation detection in MYH2 gene for Inclusion body myopathy

PreTest Information

Clinical History of Patient who is going for MYH2 Gene Inclusion body myopathy NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MYH2 Gene Inclusion body myopathy

Detail Description

MYH2 Gene Inclusion Body Myopathy NGS Genetic DNA Test Cost INR:20000 Symptoms Diagnosis

Inclusion body myopathy (IBM) is a rare genetic disorder that affects the muscles. It is caused by mutations in various genes, including the MYH2 gene. The MYH2 gene provides instructions for making a protein called myosin heavy chain IIa, which is found in muscle fibers that are responsible for generating force and movement. Mutations in the MYH2 gene can lead to the development of inclusion body myopathy, a progressive muscle disorder that typically begins in adulthood and is characterized by muscle weakness and wasting.

Symptoms of MYH2 Gene Inclusion Body Myopathy

The symptoms of MYH2 gene inclusion body myopathy can vary widely from person to person. Some people may experience only mild weakness, while others may be severely affected and require assistance with daily activities. The most common symptoms of MYH2 gene inclusion body myopathy include:

• Weakness in the muscles of the arms and legs
• Difficulty walking
• Difficulty standing up from a seated position
• Frequent falls
• Difficulty swallowing
• Speech difficulties

Diagnosis of MYH2 Gene Inclusion Body Myopathy

MYH2 gene inclusion body myopathy is typically diagnosed through a combination of physical examination, genetic testing, and muscle biopsy. During a physical examination, a doctor will look for signs of muscle weakness and wasting. Genetic testing can confirm the presence of mutations in the MYH2 gene, while a muscle biopsy can provide additional information about the nature and severity of the muscle damage.

NGS Genetic DNA Test for MYH2 Gene Inclusion Body Myopathy

NGS (next-generation sequencing) genetic DNA testing is a powerful diagnostic tool that can detect mutations in the MYH2 gene and other genes associated with inclusion body myopathy. This type of testing uses advanced sequencing technology to analyze the entire DNA sequence of a patient's genes, allowing for a more comprehensive analysis of genetic mutations that may be contributing to the development of the disorder.

Cost of MYH2 Gene Inclusion Body Myopathy NGS Genetic DNA Test

The cost of MYH2 gene inclusion body myopathy NGS genetic DNA testing can vary depending on the specific testing provider and the extent of the analysis required. However, on average, this type of testing typically costs around INR 20,000.

Conclusion

MYH2 gene inclusion body myopathy is a rare genetic disorder that can cause muscle weakness and wasting. Early diagnosis is essential for managing the symptoms of this condition and preventing further muscle damage. NGS genetic DNA testing is a powerful diagnostic tool that can detect mutations in the MYH2 gene and other genes associated with inclusion body myopathy, providing patients with a more comprehensive understanding of their condition. While the cost of this testing can vary, it is a worthwhile investment for those seeking a definitive diagnosis and effective treatment plan.

If you or a loved one are experiencing symptoms of MYH2 gene inclusion body myopathy, contact DNA Labs India today to schedule a consultation and learn more about NGS genetic DNA testing.

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 MYH2 Gene Inclusion body myopathy NGS Genetic DNA Test