COX6A1 Gene CMTRID Genetic Test
At DNA Labs UAE, we offer the COX6A1 Gene CMTRID Genetic Test for individuals who may be experiencing neurological disorders. This test can help diagnose, provide prognosis, and aid in treatment planning for mitochondrial diseases.
Test Details
The COX6A1 gene is a nuclear gene that encodes a subunit of cytochrome c oxidase, which plays a crucial role in the electron transport chain in mitochondria. Mutations in this gene have been linked to various mitochondrial disorders, such as Leigh syndrome and mitochondrial encephalomyopathy.
Our CMTRID NGS genetic test utilizes next-generation sequencing technology to analyze the entire mitochondrial genome and selected nuclear genes associated with mitochondrial disorders, including the COX6A1 gene. By identifying mutations in these genes, we can determine if they are responsible for mitochondrial disease, allowing for accurate diagnosis, prognosis, and treatment planning.
Components
- Test Name: COX6A1 Gene CMTRID 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
Prior to undergoing the COX6A1 Gene CMTRID NGS Genetic DNA Test, it is essential to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by COX6A1 Gene CMTRID. This information helps us gain a comprehensive understanding of the patient’s condition and aids in accurate testing and interpretation of results.
Cost
The cost of the COX6A1 Gene CMTRID Genetic Test is 4400.0 AED.
At DNA Labs UAE, we strive to provide accurate and reliable genetic testing services. If you suspect a mitochondrial disorder or have any concerns about your health, we recommend consulting with a neurologist who can guide you through the testing process and assist with diagnosis and treatment planning.
Test Name | COX6A1 Gene CMTRID 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 COX6A1 Gene CMTRID NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with COX6A1 Gene CMTRID |
Test Details | The COX6A1 gene is a nuclear gene that encodes a subunit of cytochrome c oxidase, which is involved in the electron transport chain in mitochondria. Mutations in this gene have been associated with various mitochondrial disorders, including Leigh syndrome and mitochondrial encephalomyopathy. The CMTRID NGS genetic test is a next-generation sequencing test that analyzes the entire mitochondrial genome and selected nuclear genes that are associated with mitochondrial disorders, including the COX6A1 gene. This test can identify mutations in these genes that may be responsible for mitochondrial disease and can help with diagnosis, prognosis, and treatment planning. |