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MT-TA Gene Mitochondrial myopathy MT-TA related Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The MT-TA gene is crucial for mitochondrial function, which is essential for energy production in cells. Mutations in this gene can lead to mitochondrial myopathy, a condition characterized by muscle weakness and other systemic symptoms due to the impaired function of mitochondria. Mitochondrial myopathy MT-TA related genetic testing is a specialized diagnostic tool designed to identify mutations in the MT-TA gene, confirming a diagnosis and aiding in the management of the condition.

This genetic test is performed at DNA Labs UAE, a leading facility in genetic diagnostics. The test involves collecting a DNA sample, usually through a blood draw or cheek swab, and analyzing it for specific mutations in the MT-TA gene that are known to cause mitochondrial myopathy. The results can provide valuable information for patients and their families regarding the nature of the disease, potential treatment options, and the risk of passing the condition on to future generations.

The cost of the mitochondrial myopathy MT-TA related genetic test at DNA Labs UAE is 4400 AED. This price reflects the sophisticated technology and expertise required to accurately identify mutations in the MT-TA gene. While the cost may seem significant, the information gained from this test can be invaluable for affected individuals and their healthcare providers in developing a comprehensive management plan for mitochondrial myopathy.

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MT-TA Gene Mitochondrial Myopathy Genetic Test

Test Name: MT-TA Gene Mitochondrial Myopathy MT-TA related Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

Report Delivery: 3 to 4 Weeks

Method: NGS Technology

Test Type: Cardiovascular Pneumology Disorders

Doctor: Cardiologist

Test Department: Genetics

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

Test Details

MT-TA gene mitochondrial myopathy is a rare genetic disorder characterized by muscle weakness and wasting. It is caused by mutations in the MT-TA gene, which is located in the mitochondrial DNA.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of MT-TA gene mitochondrial myopathy, NGS genetic testing can be used to identify mutations in the MT-TA gene that may be responsible for the disorder.

NGS genetic testing typically involves obtaining a DNA sample from the individual undergoing testing, which can be done through a blood sample or a cheek swab. The DNA sample is then sequenced using NGS technology, and the resulting data is analyzed to identify any mutations or variations in the MT-TA gene.

The results of the NGS genetic test can help confirm a diagnosis of MT-TA gene mitochondrial myopathy and provide information about the specific genetic mutation involved. This information can be useful for genetic counseling, family planning, and potentially for guiding treatment decisions in the future.

It is important to note that genetic testing for MT-TA gene mitochondrial myopathy is typically ordered by a healthcare professional with expertise in genetics. The results of the test should be interpreted in the context of the individual’s clinical symptoms and family history. Genetic counseling is often recommended both before and after genetic testing to ensure a thorough understanding of the implications and limitations of the test results.

Test Name MT-TA Gene Mitochondrial myopathy MT-TA related Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Cardiovascular Pneumology Disorders
Doctor Cardiologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for MT-TA Gene Mitochondrial myopathy, MT-TA related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MT-TA Gene Mitochondrial myopathy, MT-TA related NGS Genetic DNA Test gene MT-TA
Test Details

MT-TA gene mitochondrial myopathy is a rare genetic disorder characterized by muscle weakness and wasting. It is caused by mutations in the MT-TA gene, which is located in the mitochondrial DNA.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of MT-TA gene mitochondrial myopathy, NGS genetic testing can be used to identify mutations in the MT-TA gene that may be responsible for the disorder.

NGS genetic testing typically involves obtaining a DNA sample from the individual undergoing testing, which can be done through a blood sample or a cheek swab. The DNA sample is then sequenced using NGS technology, and the resulting data is analyzed to identify any mutations or variations in the MT-TA gene.

The results of the NGS genetic test can help confirm a diagnosis of MT-TA gene mitochondrial myopathy and provide information about the specific genetic mutation involved. This information can be useful for genetic counseling, family planning, and potentially for guiding treatment decisions in the future.

It is important to note that genetic testing for MT-TA gene mitochondrial myopathy is typically ordered by a healthcare professional with expertise in genetics. The results of the test should be interpreted in the context of the individual’s clinical symptoms and family history. Genetic counseling is often recommended both before and after genetic testing to ensure a thorough understanding of the implications and limitations of the test results.