NDUFS4 Gene Mitochondrial Complex I Deficiency Genetic Test
Components:
- Test Name: NDUFS4 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 NDUFS4 Gene Mitochondrial Complex I Deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFS4 Gene Mitochondrial Complex I Deficiency.
Test Details:
NDUFS4 gene mitochondrial complex I deficiency is a rare genetic disorder that affects the function of mitochondria, the energy-producing structures within cells. This condition is caused by mutations in the NDUFS4 gene, which provides instructions for making a protein that is a subunit of complex I, an essential component of the mitochondrial electron transport chain.
A next-generation sequencing (NGS) genetic test can be used to identify mutations in the NDUFS4 gene. NGS is a high-throughput sequencing technology that allows for the rapid and simultaneous sequencing of multiple genes or even the entire genome. It can detect various types of genetic variations, including small point mutations, insertions, deletions, and duplications.
The NGS genetic test for NDUFS4 gene mitochondrial complex I deficiency involves collecting a sample of DNA, usually through a blood or saliva sample. The DNA is then sequenced using NGS technology, and the resulting data is analyzed to identify any mutations or variations in the NDUFS4 gene.
The test results can help confirm a diagnosis of NDUFS4 gene mitochondrial complex I deficiency and provide information about the specific genetic mutation causing the condition. This information can be valuable for understanding the underlying cause of the disorder, predicting disease progression, and informing potential treatment options.
It is important to note that genetic testing should be done in consultation with a healthcare professional or genetic counselor who can provide guidance on the implications of the test results and help interpret them in the context of an individual’s specific situation.
| Test Name | NDUFS4 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 NDUFS4 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFS4 Gene Mitochondrial complex I deficiency |
| Test Details |
NDUFS4 gene mitochondrial complex I deficiency is a rare genetic disorder that affects the function of mitochondria, the energy-producing structures within cells. This condition is caused by mutations in the NDUFS4 gene, which provides instructions for making a protein that is a subunit of complex I, an essential component of the mitochondrial electron transport chain. A next-generation sequencing (NGS) genetic test can be used to identify mutations in the NDUFS4 gene. NGS is a high-throughput sequencing technology that allows for the rapid and simultaneous sequencing of multiple genes or even the entire genome. It can detect various types of genetic variations, including small point mutations, insertions, deletions, and duplications. The NGS genetic test for NDUFS4 gene mitochondrial complex I deficiency involves collecting a sample of DNA, usually through a blood or saliva sample. The DNA is then sequenced using NGS technology, and the resulting data is analyzed to identify any mutations or variations in the NDUFS4 gene. The test results can help confirm a diagnosis of NDUFS4 gene mitochondrial complex I deficiency and provide information about the specific genetic mutation causing the condition. This information can be valuable for understanding the underlying cause of the disorder, predicting disease progression, and informing potential treatment options. It is important to note that genetic testing should be done in consultation with a healthcare professional or genetic counselor who can provide guidance on the implications of the test results and help interpret them in the context of an individual’s specific situation. |
