MT-TF Gene MELAS Syndrome Genetic Test
At DNA Labs UAE, we offer the MT-TF Gene MELAS syndrome Genetic Test at a cost of AED 4400.0. This test focuses on analyzing the MT-TF gene for mutations associated with MELAS syndrome, a rare mitochondrial disorder that affects multiple organ systems.
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
Before undergoing the MT-TF Gene MELAS syndrome Genetic Test, it is important to provide the clinical history of the patient. A genetic counseling session is also recommended to draw a pedigree chart of family members affected with MT-TF Gene MELAS syndrome NGS Genetic DNA Test gene MT-TF.
Test Details
The MT-TF gene MELAS syndrome NGS genetic test is a type of genetic test that focuses on analyzing the MT-TF gene for mutations associated with MELAS syndrome. MELAS syndrome is a rare mitochondrial disorder that affects the brain and muscles. The NGS technology used in this test allows for the simultaneous analysis of multiple genes, including the MT-TF gene, to identify any genetic variations or mutations that may be present. This can help in confirming a diagnosis of MELAS syndrome and understanding the underlying genetic cause of the condition.
The MT-TF gene is responsible for providing instructions to produce a specific protein involved in mitochondrial function. Mutations in this gene can disrupt the normal functioning of mitochondria, leading to the symptoms associated with MELAS syndrome. By identifying mutations in the MT-TF gene, the NGS genetic test can assist in the early detection, diagnosis, and management of MELAS syndrome. It can also help in providing information about the inheritance pattern of the condition, allowing for genetic counseling and family planning decisions.
It is important to note that this genetic test is typically ordered by a healthcare professional, such as a geneticist or a neurologist, who specializes in mitochondrial disorders. The results of the test are usually interpreted in conjunction with the individual’s clinical symptoms and medical history to provide a comprehensive diagnosis and appropriate treatment recommendations.
| Test Name | MT-TF Gene MELAS syndrome 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-TF Gene MELAS syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MT-TF Gene MELAS syndrome NGS Genetic DNA Test gene MT-TF |
| Test Details |
MT-TF gene MELAS syndrome NGS genetic test is a type of genetic test that focuses on analyzing the MT-TF gene for mutations associated with MELAS syndrome. MELAS syndrome (Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like episodes) is a rare mitochondrial disorder that affects multiple organ systems, particularly the brain and muscles. The NGS (Next-Generation Sequencing) technology used in this test allows for the simultaneous analysis of multiple genes, including the MT-TF gene, to identify any genetic variations or mutations that may be present. This can help in confirming a diagnosis of MELAS syndrome and understanding the underlying genetic cause of the condition. The MT-TF gene is responsible for providing instructions to produce a specific protein involved in mitochondrial function. Mutations in this gene can disrupt the normal functioning of mitochondria, leading to the symptoms associated with MELAS syndrome. By identifying mutations in the MT-TF gene, the NGS genetic test can assist in the early detection, diagnosis, and management of MELAS syndrome. It can also help in providing information about the inheritance pattern of the condition, allowing for genetic counseling and family planning decisions. It is important to note that this genetic test is typically ordered by a healthcare professional, such as a geneticist or a neurologist, who specializes in mitochondrial disorders. The results of the test are usually interpreted in conjunction with the individual’s clinical symptoms and medical history to provide a comprehensive diagnosis and appropriate treatment recommendations. |
