LRPPRC Gene Leigh Syndrome French-Canadian Type Genetic Test
Components: LRPPRC Gene Leigh syndrome French-Canadian type 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 LRPPRC Gene Leigh syndrome, French-Canadian type NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with LRPPRC Gene Leigh syndrome, French-Canadian type.
Test Details:
The LRPPRC gene is associated with Leigh syndrome, which is a rare genetic disorder characterized by progressive neurological degeneration. The French-Canadian type refers to a specific variant of Leigh syndrome that is more prevalent in the French-Canadian population.
NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously and identify genetic variations or mutations that may be associated with a particular condition. In the case of LRPPRC gene Leigh syndrome, NGS genetic testing can be used to identify mutations in the LRPPRC gene that are responsible for causing the disorder.
NGS genetic testing involves sequencing the DNA of an individual to identify any variations or mutations in the LRPPRC gene. This can help in diagnosing Leigh syndrome and determining the specific genetic cause of the condition. It can also be used for carrier testing in individuals with a family history of Leigh syndrome to assess the risk of passing on the condition to their children.
It is important to consult with a genetic counselor or healthcare professional before undergoing any genetic testing. They can provide guidance on the appropriateness of the test, its potential benefits, limitations, and implications, as well as help interpret the results and provide appropriate counseling and support.
| Test Name | LRPPRC Gene Leigh syndrome French-Canadian type 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 LRPPRC Gene Leigh syndrome, French-Canadian type NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with LRPPRC Gene Leigh syndrome, French-Canadian type |
| Test Details |
The LRPPRC gene is associated with Leigh syndrome, which is a rare genetic disorder characterized by progressive neurological degeneration. The French-Canadian type refers to a specific variant of Leigh syndrome that is more prevalent in the French-Canadian population. NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously and identify genetic variations or mutations that may be associated with a particular condition. In the case of LRPPRC gene Leigh syndrome, NGS genetic testing can be used to identify mutations in the LRPPRC gene that are responsible for causing the disorder. NGS genetic testing involves sequencing the DNA of an individual to identify any variations or mutations in the LRPPRC gene. This can help in diagnosing Leigh syndrome and determining the specific genetic cause of the condition. It can also be used for carrier testing in individuals with a family history of Leigh syndrome to assess the risk of passing on the condition to their children. It is important to consult with a genetic counselor or healthcare professional before undergoing any genetic testing. They can provide guidance on the appropriateness of the test, its potential benefits, limitations, and implications, as well as help interpret the results and provide appropriate counseling and support. |
