NDUFA1 Gene Mitochondrial Complex I Deficiency Genetic Test
Test Name: NDUFA1 Gene Mitochondrial Complex I Deficiency Genetic Test
Components: NGS Technology
Price: 4400.0 AED
Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery: 3 to 4 Weeks
Test Type: Neurological Disorders
Doctor: Neurologist
Test Department: Genetics
Pre Test Information: Clinical History of Patient who is going for NDUFA1 Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFA1 Gene Mitochondrial Complex I Deficiency.
Test Details
The NDUFA1 gene is one of the many genes involved in the production of mitochondrial complex I, which is an essential enzyme complex involved in the process of cellular respiration. Mutations in the NDUFA1 gene can lead to mitochondrial complex I deficiency, which is a rare genetic disorder characterized by impaired energy production in cells.
NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can be used to identify mutations in genes, including the NDUFA1 gene. NGS allows for the simultaneous analysis of multiple genes, making it a powerful tool for identifying the genetic cause of complex disorders like mitochondrial complex I deficiency.
The NGS genetic test for NDUFA1 gene mutations involves sequencing the DNA of an individual to identify any changes or mutations in the gene. This can help in diagnosing mitochondrial complex I deficiency and determining the specific genetic cause of the disorder in an affected individual. Genetic testing can also be used for carrier testing in individuals with a family history of the disorder.
It is important to note that genetic testing for mitochondrial complex I deficiency may not be widely available and may require consultation with a geneticist or a specialized laboratory that offers such testing. Additionally, the interpretation of genetic test results should be done by a healthcare professional with expertise in genetics.
| Test Name | NDUFA1 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 NDUFA1 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFA1 Gene Mitochondrial complex I deficiency |
| Test Details |
The NDUFA1 gene is one of the many genes involved in the production of mitochondrial complex I, which is an essential enzyme complex involved in the process of cellular respiration. Mutations in the NDUFA1 gene can lead to mitochondrial complex I deficiency, which is a rare genetic disorder characterized by impaired energy production in cells. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can be used to identify mutations in genes, including the NDUFA1 gene. NGS allows for the simultaneous analysis of multiple genes, making it a powerful tool for identifying the genetic cause of complex disorders like mitochondrial complex I deficiency. The NGS genetic test for NDUFA1 gene mutations involves sequencing the DNA of an individual to identify any changes or mutations in the gene. This can help in diagnosing mitochondrial complex I deficiency and determining the specific genetic cause of the disorder in an affected individual. Genetic testing can also be used for carrier testing in individuals with a family history of the disorder. It is important to note that genetic testing for mitochondrial complex I deficiency may not be widely available and may require consultation with a geneticist or a specialized laboratory that offers such testing. Additionally, the interpretation of genetic test results should be done by a healthcare professional with expertise in genetics. |
