MT-CO1 Gene Cytochrome c oxidase 1 deficiency Genetic Test
Test Name: MT-CO1 Gene Cytochrome c oxidase 1 deficiency Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
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-CO1 Gene Cytochrome c oxidase 1 deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MT-CO1 Gene Cytochrome c oxidase 1 deficiency
Test Details
The MT-CO1 gene encodes for the cytochrome c oxidase subunit 1, which is an essential component of the mitochondrial respiratory chain. Cytochrome c oxidase 1 deficiency is a rare genetic disorder that affects the function of this enzyme, leading to impaired energy production and mitochondrial dysfunction.
NGS (Next-Generation Sequencing) genetic testing is a powerful tool that can be used to identify mutations in the MT-CO1 gene that cause cytochrome c oxidase 1 deficiency. This test involves sequencing the entire coding region of the MT-CO1 gene and analyzing the data for genetic variations that may be associated with the disorder.
NGS genetic testing for cytochrome c oxidase 1 deficiency can help to confirm a diagnosis, provide information about the severity of the condition, and guide treatment decisions. It may also be used to identify carriers of the genetic mutation, which can be useful for family planning purposes.
Overall, NGS genetic testing for MT-CO1 gene mutations is an important tool for the diagnosis and management of cytochrome c oxidase 1 deficiency, a rare genetic disorder that can have significant impacts on affected individuals and their families.
| Test Name | MT-CO1 Gene Cytochrome c oxidase 1 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-CO1 Gene Cytochrome c oxidase 1 deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MT-CO1 Gene Cytochrome c oxidase 1 deficiency |
| Test Details | MT-CO1 gene encodes for the cytochrome c oxidase subunit 1, which is an essential component of the mitochondrial respiratory chain. Cytochrome c oxidase 1 deficiency is a rare genetic disorder that affects the function of this enzyme, leading to impaired energy production and mitochondrial dysfunction. NGS (Next-Generation Sequencing) genetic testing is a powerful tool that can be used to identify mutations in the MT-CO1 gene that cause cytochrome c oxidase 1 deficiency. This test involves sequencing the entire coding region of the MT-CO1 gene and analyzing the data for genetic variations that may be associated with the disorder. NGS genetic testing for cytochrome c oxidase 1 deficiency can help to confirm a diagnosis, provide information about the severity of the condition, and guide treatment decisions. It may also be used to identify carriers of the genetic mutation, which can be useful for family planning purposes. Overall, NGS genetic testing for MT-CO1 gene mutations is an important tool for the diagnosis and management of cytochrome c oxidase 1 deficiency, a rare genetic disorder that can have significant impacts on affected individuals and their families. |
