NDUFAF3 Gene Mitochondrial Complex I Deficiency Genetic Test
At DNA Labs UAE, we offer the NDUFAF3 Gene Mitochondrial Complex I Deficiency Genetic Test to help diagnose neurological disorders. This test analyzes the NDUFAF3 gene, which is responsible for encoding a protein called NADH dehydrogenase (ubiquinone) complex I assembly factor 3.
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 NDUFAF3 Gene Mitochondrial Complex I Deficiency Genetic Test, it is important 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 with NDUFAF3 Gene Mitochondrial Complex I Deficiency. This will help in understanding the inheritance pattern and identifying potential carriers of the mutation.
Test Details
Mitochondrial complex I is a large protein complex located in the inner mitochondrial membrane. It is responsible for the first step in the electron transport chain, which is essential for energy production in cells. The NDUFAF3 gene plays a crucial role in the assembly and stability of mitochondrial complex I.
NGS (Next-Generation Sequencing) genetic testing is utilized to analyze multiple genes simultaneously and identify genetic variations or mutations. In the case of mitochondrial complex I deficiency, NGS genetic testing can detect mutations in the NDUFAF3 gene that may be causing the deficiency.
By identifying specific mutations in the NDUFAF3 gene, NGS genetic testing aids in the diagnosis of mitochondrial complex I deficiency and determining the underlying cause of the condition. This information is valuable for understanding disease progression, predicting prognosis, and guiding treatment options.
Don’t wait any longer to get the answers you need. Contact DNA Labs UAE today to schedule your NDUFAF3 Gene Mitochondrial Complex I Deficiency Genetic Test.
| Test Name | NDUFAF3 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 NDUFAF3 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFAF3 Gene Mitochondrial complex I deficiency |
| Test Details |
The NDUFAF3 gene is responsible for encoding a protein called NADH dehydrogenase (ubiquinone) complex I assembly factor 3. This protein is involved in the assembly and stability of mitochondrial complex I, which is a large protein complex located in the inner mitochondrial membrane. Mitochondrial complex I is responsible for the first step in the electron transport chain, which is the process by which cells generate energy in the form of ATP. Mutations in the NDUFAF3 gene can lead to a deficiency in mitochondrial complex I, resulting in impaired energy production. NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously to identify genetic variations or mutations. In the case of mitochondrial complex I deficiency, NGS genetic testing can be used to identify mutations in the NDUFAF3 gene that may be causing the deficiency. By identifying specific mutations in the NDUFAF3 gene, NGS genetic testing can help in diagnosing mitochondrial complex I deficiency and determining the underlying cause of the condition. This information can be valuable for understanding the disease progression, predicting the prognosis, and potentially guiding treatment options. |
