GALC Gene Krabbe Disease Genetic Test
Cost: AED 4400.0
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: Metabolic Disorders
- Doctor: General Physician
- Test Department: Genetics
Pre Test Information:
Clinical History of Patient who is going for GALC Gene Krabbe disease NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Krabbe disease.
Test Details:
The GALC (galactosylceramidase) gene is associated with Krabbe disease, also known as globoid cell leukodystrophy. This is a rare genetic disorder characterized by the progressive destruction of the myelin sheath in the nervous system.
NGS (next-generation sequencing) is a type of genetic testing method that allows for the rapid sequencing of multiple genes simultaneously. In the case of Krabbe disease, NGS genetic testing can be used to identify mutations or variants in the GALC gene that may be causing the disease.
NGS testing can help in the diagnosis of Krabbe disease by identifying specific mutations in the GALC gene that are known to be associated with the condition. This can provide important information for genetic counseling, family planning, and potential treatment options.
It is important to note that while NGS testing can be a powerful tool in diagnosing genetic disorders like Krabbe disease, it is not a cure or treatment in itself. Treatment options for Krabbe disease are limited, and typically involve supportive care to manage symptoms and slow disease progression.
If you suspect that you or someone you know may have Krabbe disease, it is recommended to consult with a healthcare professional or a genetic counselor who can provide more information about genetic testing options and appropriate next steps.
| Test Name | GALC Gene Krabbe disease Genetic 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 | Metabolic Disorders |
| Doctor | General Physician |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for GALC Gene Krabbe disease NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Krabbe disease |
| Test Details |
GALC (galactosylceramidase) gene is associated with Krabbe disease, also known as globoid cell leukodystrophy. This is a rare genetic disorder characterized by the progressive destruction of the myelin sheath in the nervous system. NGS (next-generation sequencing) is a type of genetic testing method that allows for the rapid sequencing of multiple genes simultaneously. In the case of Krabbe disease, NGS genetic testing can be used to identify mutations or variants in the GALC gene that may be causing the disease. NGS testing can help in the diagnosis of Krabbe disease by identifying specific mutations in the GALC gene that are known to be associated with the condition. This can provide important information for genetic counseling, family planning, and potential treatment options. It is important to note that while NGS testing can be a powerful tool in diagnosing genetic disorders like Krabbe disease, it is not a cure or treatment in itself. Treatment options for Krabbe disease are limited, and typically involve supportive care to manage symptoms and slow disease progression. If you suspect that you or someone you know may have Krabbe disease, it is recommended to consult with a healthcare professional or a genetic counselor who can provide more information about genetic testing options and appropriate next steps. |
