FOXRED1 Gene Mitochondrial complex I deficiency Genetic Test
Test Name: FOXRED1 Gene Mitochondrial complex I deficiency Genetic Test
Components: FOXRED1 Gene Mitochondrial complex I 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 FOXRED1 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FOXRED1 Gene Mitochondrial complex I deficiency.
Test Details:
The FOXRED1 gene is responsible for encoding a protein called FOXRED1, which is involved in the assembly and function of mitochondrial complex I. Mitochondrial complex I is a large protein complex that plays a crucial role in the process of oxidative phosphorylation, which is responsible for generating energy in the form of ATP in the mitochondria.
Mutations in the FOXRED1 gene can lead to mitochondrial complex I deficiency, which is a rare genetic disorder characterized by a wide range of symptoms. These symptoms can include developmental delay, muscle weakness, seizures, intellectual disability, and various neurological problems.
NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of mitochondrial complex I deficiency, NGS genetic testing can be used to identify mutations in the FOXRED1 gene, as well as other genes known to be associated with mitochondrial complex I deficiency.
By identifying the specific genetic mutations causing mitochondrial complex I deficiency, NGS genetic testing can help in the diagnosis and management of the condition. It can also provide valuable information for genetic counseling and family planning.
Test Name | FOXRED1 Gene Mitochondrial complex I 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 FOXRED1 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with FOXRED1 Gene Mitochondrial complex I deficiency |
Test Details |
The FOXRED1 gene is responsible for encoding a protein called FOXRED1, which is involved in the assembly and function of mitochondrial complex I. Mitochondrial complex I is a large protein complex that plays a crucial role in the process of oxidative phosphorylation, which is responsible for generating energy in the form of ATP in the mitochondria. Mutations in the FOXRED1 gene can lead to mitochondrial complex I deficiency, which is a rare genetic disorder characterized by a wide range of symptoms. These symptoms can include developmental delay, muscle weakness, seizures, intellectual disability, and various neurological problems. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of mitochondrial complex I deficiency, NGS genetic testing can be used to identify mutations in the FOXRED1 gene, as well as other genes known to be associated with mitochondrial complex I deficiency. By identifying the specific genetic mutations causing mitochondrial complex I deficiency, NGS genetic testing can help in the diagnosis and management of the condition. It can also provide valuable information for genetic counseling and family planning. |