BCS1L Gene Leigh syndrome Genetic Test
Test Components
- 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 BCS1L Gene Leigh syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with BCS1L Gene Leigh syndrome.
Test Details
The BCS1L gene is associated with a rare genetic disorder called Leigh syndrome. Leigh syndrome is a severe neurological disorder that typically presents in infancy or early childhood and is characterized by progressive loss of mental and movement abilities. It is caused by mutations in various genes, including BCS1L.
Next-generation sequencing (NGS) is a genetic testing method that allows for the analysis of multiple genes simultaneously. In the context of Leigh syndrome, NGS can be used to identify mutations in the BCS1L gene or other genes associated with the disorder. This can help in confirming a diagnosis, predicting the prognosis, and providing genetic counseling to affected individuals and their families.
The BCS1L gene Leigh syndrome NGS genetic test involves obtaining a DNA sample, usually through a blood sample, from the individual suspected of having Leigh syndrome. The DNA is then sequenced using NGS technology to identify any mutations or variations in the BCS1L gene. The results of the test can help guide treatment decisions and provide information about the risk of passing on the condition to future generations.
It is important to note that genetic testing for Leigh syndrome and other genetic disorders should be conducted by a qualified healthcare professional or genetic counselor. They can provide appropriate counseling and support throughout the testing process and help interpret the results.
| Test Name | BCS1L Gene Leigh syndrome 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 BCS1L Gene Leigh syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with BCS1L Gene Leigh syndrome |
| Test Details | The BCS1L gene is associated with a rare genetic disorder called Leigh syndrome. Leigh syndrome is a severe neurological disorder that typically presents in infancy or early childhood and is characterized by progressive loss of mental and movement abilities. It is caused by mutations in various genes, including BCS1L. Next-generation sequencing (NGS) is a genetic testing method that allows for the analysis of multiple genes simultaneously. In the context of Leigh syndrome, NGS can be used to identify mutations in the BCS1L gene or other genes associated with the disorder. This can help in confirming a diagnosis, predicting the prognosis, and providing genetic counseling to affected individuals and their families. The BCS1L gene Leigh syndrome NGS genetic test involves obtaining a DNA sample, usually through a blood sample, from the individual suspected of having Leigh syndrome. The DNA is then sequenced using NGS technology to identify any mutations or variations in the BCS1L gene. The results of the test can help guide treatment decisions and provide information about the risk of passing on the condition to future generations. It is important to note that genetic testing for Leigh syndrome and other genetic disorders should be conducted by a qualified healthcare professional or genetic counselor. They can provide appropriate counseling and support throughout the testing process and help interpret the results. |
