NDUFAF4 Gene Mitochondrial Complex I Deficiency Genetic Test
Welcome to DNA Labs UAE, where we offer the NDUFAF4 Gene Mitochondrial Complex I Deficiency Genetic Test. This test is designed to diagnose individuals with suspected symptoms or a family history of mitochondrial complex I deficiency. Read on to learn more about the test components, price, sample condition, report delivery time, testing method, test type, referring doctor, test department, pre-test information, and test details.
Test Components
- NDUFAF4 Gene Mitochondrial Complex I Deficiency Genetic Test
Price
AED 4400.0
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
Referring Doctor
Neurologist
Test Department
Genetics
Pre Test Information
Prior to undergoing the NDUFAF4 Gene Mitochondrial Complex I Deficiency Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by NDUFAF4 Gene Mitochondrial Complex I Deficiency.
Test Details
The NDUFAF4 gene is responsible for coding a protein involved in the function of mitochondrial complex I. This enzyme complex plays a crucial role in the electron transport chain of mitochondria. Mutations in the NDUFAF4 gene can result in mitochondrial complex I deficiency, a genetic disorder characterized by impaired energy production in cells.
NGS (Next-Generation Sequencing) genetic testing is utilized to analyze multiple genes simultaneously, including the NDUFAF4 gene and other genes associated with mitochondrial function. By using NGS genetic testing, mutations in the NDUFAF4 gene can be identified, aiding in the diagnosis of mitochondrial complex I deficiency. This test can also provide information about the specific genetic mutation causing the disorder, which can be valuable for genetic counseling and family planning.
In conclusion, the NDUFAF4 Gene Mitochondrial Complex I Deficiency Genetic Test offered by DNA Labs UAE is an essential tool for diagnosing and managing this genetic disorder. By identifying mutations in the NDUFAF4 gene and other genes involved in mitochondrial complex I deficiency, this test contributes to better patient care and informed decision-making.
Test Name | NDUFAF4 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 NDUFAF4 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFAF4 Gene Mitochondrial complex I deficiency |
Test Details |
The NDUFAF4 gene is a gene that codes for a protein involved in the function of mitochondrial complex I, which is a key enzyme complex in the electron transport chain of mitochondria. Mutations in the NDUFAF4 gene can lead to mitochondrial complex I deficiency, which is a genetic disorder characterized by impaired energy production in cells. NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously to identify genetic variations or mutations. In the context of mitochondrial complex I deficiency, NGS genetic testing can be used to identify mutations in the NDUFAF4 gene and other genes associated with mitochondrial function. NGS genetic testing for mitochondrial complex I deficiency can help diagnose the condition in individuals with suspected symptoms or family history. It can also provide information about the specific genetic mutation causing the disorder, which can be useful for genetic counseling and family planning. Overall, NGS genetic testing for the NDUFAF4 gene and other genes involved in mitochondrial complex I deficiency can aid in the diagnosis and management of this genetic disorder. |