MT-CO3 Gene Cytochrome c oxidase 3 deficiency Genetic Test
Components: MT-CO3 Gene Cytochrome c oxidase 3 deficiency Genetic Test
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: Neurological Disorders
Doctor: Neurologist
Test Department: Genetics
Pre Test Information: Clinical History of Patient who is going for MT-CO3 Gene Cytochrome c oxidase 3 deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MT-CO3 Gene Cytochrome c oxidase 3 deficiency.
Test Details
The MT-CO3 gene codes for the cytochrome c oxidase subunit III, which is a key component of the mitochondrial respiratory chain. Mutations in this gene can lead to cytochrome c oxidase 3 deficiency, which is a rare genetic disorder that affects the function of the mitochondrial respiratory chain. This can cause a range of symptoms, including muscle weakness, exercise intolerance, developmental delay, and neurological problems.
NGS genetic testing can be used to identify mutations in the MT-CO3 gene and diagnose cytochrome c oxidase 3 deficiency. This involves sequencing the entire gene to identify any variations or mutations that may be causing the disorder. NGS testing is a highly accurate and efficient method of genetic testing that can provide a definitive diagnosis for patients with suspected genetic disorders. It can also be used for carrier testing and prenatal testing in families with a history of cytochrome c oxidase 3 deficiency.
Test Name | MT-CO3 Gene Cytochrome c oxidase 3 deficiency Genetic Test |
---|---|
Components | |
Price | 4400.0 AED |
Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card o |
Report Delivery | 3 to 4 Weeks |
Method | NGS Technology |
Test type | Neurological Disorders |
Doctor | Neurologist |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for MT-CO3 Gene Cytochrome c oxidase 3 deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MT-CO3 Gene Cytochrome c oxidase 3 deficiency |
Test Details | The MT-CO3 gene codes for the cytochrome c oxidase subunit III, which is a key component of the mitochondrial respiratory chain. Mutations in this gene can lead to cytochrome c oxidase 3 deficiency, which is a rare genetic disorder that affects the function of the mitochondrial respiratory chain. This can cause a range of symptoms, including muscle weakness, exercise intolerance, developmental delay, and neurological problems. NGS genetic testing can be used to identify mutations in the MT-CO3 gene and diagnose cytochrome c oxidase 3 deficiency. This involves sequencing the entire gene to identify any variations or mutations that may be causing the disorder. NGS testing is a highly accurate and efficient method of genetic testing that can provide a definitive diagnosis for patients with suspected genetic disorders. It can also be used for carrier testing and prenatal testing in families with a history of cytochrome c oxidase 3 deficiency. |