NDUFA11 Gene Mitochondrial Complex I Deficiency Genetic Test
Welcome to DNA Labs UAE, where we offer the NDUFA11 gene mitochondrial complex I deficiency genetic test. This test is designed to diagnose and provide information about mitochondrial complex I deficiency, a genetic disorder affecting the function of the mitochondria.
Test Components and Price
- Test Name: NDUFA11 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 NDUFA11 Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFA11 Gene Mitochondrial Complex I Deficiency
About the NDUFA11 Gene and Mitochondrial Complex I Deficiency
The NDUFA11 gene is associated with mitochondrial complex I deficiency, a genetic disorder that affects the function of the mitochondria. Mitochondrial complex I is responsible for the first step in the electron transport chain, which generates energy for the cell. Mutations in the NDUFA11 gene can lead to a deficiency in complex I activity, resulting in various symptoms and health issues.
NGS Technology and Genetic Testing
NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of mitochondrial complex I deficiency, NGS genetic testing can identify mutations in the NDUFA11 gene, as well as other genes associated with complex I deficiency. This comprehensive analysis can help diagnose the condition and provide information about the specific genetic cause.
Uses of NGS Genetic Testing
NGS genetic testing can be useful for individuals with suspected mitochondrial complex I deficiency as it allows for a comprehensive analysis of multiple genes involved in the condition. It can also be used for carrier testing, prenatal testing, and genetic counseling for families with a history of the disorder.
Important Information
It is important to note that NGS genetic testing should be performed and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors, who can provide appropriate counseling and guidance based on the test results.
| Test Name | NDUFA11 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 NDUFA11 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFA11 Gene Mitochondrial complex I deficiency |
| Test Details |
The NDUFA11 gene is associated with mitochondrial complex I deficiency, which is a genetic disorder affecting the function of the mitochondria. Mitochondrial complex I is responsible for the first step in the electron transport chain, which generates energy for the cell. Mutations in the NDUFA11 gene can lead to a deficiency in complex I activity, resulting in a variety of symptoms and health issues. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of mitochondrial complex I deficiency, NGS genetic testing can identify mutations in the NDUFA11 gene, as well as other genes associated with complex I deficiency. This can help in the diagnosis of the condition and provide information about the specific genetic cause. NGS genetic testing can be useful for individuals with suspected mitochondrial complex I deficiency, as it allows for a comprehensive analysis of multiple genes involved in the condition. It can also be used for carrier testing, prenatal testing, and genetic counseling for families with a history of the disorder. It is important to note that NGS genetic testing should be performed and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors, who can provide appropriate counseling and guidance based on the test results. |