Short Description

NGS genetic DNA test detecets for variant and mutation detection in MT-TM gene for Mitochondrial myopathy, MT-TM related

PreTest Information

Clinical History of Patient who is going for MT-TM Gene Mitochondrial myopathy, MT-TM related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MT-TM Gene Mitochondrial myopathy, MT-TM related NGS Genetic DNA Test gene MT-TM

Detail Description

MT-TM Gene Mitochondrial Myopathy: Symptoms, Diagnosis, and NGS Genetic DNA Test Cost in India

Mitochondrial myopathy is a rare genetic disorder that affects the mitochondria, which are the energy-producing organelles in our cells. The MT-TM gene is one of the genes that can cause mitochondrial myopathy when it has mutations.

Symptoms of MT-TM Gene Mitochondrial Myopathy

The symptoms of MT-TM gene mitochondrial myopathy can vary from person to person. Some common symptoms include:

• Muscle weakness and fatigue
• Exercise intolerance
• Difficulty swallowing
• Vision and hearing problems
• Developmental delays in children

These symptoms can appear at any age, but they often develop in childhood or early adulthood.

Diagnosis of MT-TM Gene Mitochondrial Myopathy

Diagnosing MT-TM gene mitochondrial myopathy can be challenging, as the symptoms are similar to those of other neuromuscular disorders. However, there are several tests that can help confirm a diagnosis:

• Muscle biopsy: A small sample of muscle tissue is taken and examined under a microscope to look for abnormalities in the mitochondria.
• Blood tests: These can measure the levels of certain enzymes and proteins that are associated with mitochondrial function.
• Genetic testing: This can identify mutations in the MT-TM gene that are causing the disorder.

It's important to get an accurate diagnosis, as this can help guide treatment and management of the disorder.

NGS Genetic DNA Test Cost for MT-TM Gene Mitochondrial Myopathy in India

Next-generation sequencing (NGS) is a type of genetic testing that can analyze multiple genes at once, including the MT-TM gene. This can provide a more comprehensive diagnosis of mitochondrial myopathy.

The cost of an NGS genetic DNA test for MT-TM gene mitochondrial myopathy in India is around INR 20,000. However, the cost can vary depending on the specific testing facility and any additional tests that may be needed.

Conclusion

MT-TM gene mitochondrial myopathy is a rare genetic disorder that can cause a range of symptoms, including muscle weakness and fatigue, exercise intolerance, and vision and hearing problems. Diagnosis can be challenging, but a combination of tests, including genetic testing, can help confirm the disorder. Next-generation sequencing is a useful tool for analyzing multiple genes at once and can provide a more comprehensive diagnosis. The cost of an NGS genetic DNA test for MT-TM gene mitochondrial myopathy in India is around INR 20,000.

If you are experiencing any symptoms of mitochondrial myopathy, it's important to see a healthcare professional for an accurate diagnosis and appropriate treatment.

For more information about genetic testing for mitochondrial myopathy and other disorders, contact DNA Labs India.

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 MT-TM Gene Mitochondrial myopathy, MT-TM related NGS Genetic DNA Test