TFG Gene SPG57 Genetic Test
Components: TFG Gene SPG57 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 TFG Gene SPG57 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TFG Gene SPG57.
Test Details: The TFG gene is associated with hereditary spastic paraplegia type 57 (SPG57), which is a rare genetic disorder characterized by progressive stiffness and weakness of the lower limbs. NGS stands for Next-Generation Sequencing, which is a high-throughput DNA sequencing technology that allows for the analysis of multiple genes simultaneously. The TFG SPG57 NGS genetic test is a diagnostic test that uses next-generation sequencing to analyze the TFG gene for any disease-causing mutations. This test can help confirm a diagnosis of SPG57 in individuals with suspected hereditary spastic paraplegia and can also be used for carrier testing in individuals with a family history of the condition. The results of the TFG SPG57 NGS genetic test can provide valuable information for genetic counseling, family planning, and potential treatment options. It is important to consult with a healthcare professional or genetic counselor to understand the implications and limitations of the test results.
Test Name | TFG Gene SPG57 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 TFG Gene SPG57 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with TFG Gene SPG57 |
Test Details |
The TFG gene is associated with hereditary spastic paraplegia type 57 (SPG57), which is a rare genetic disorder characterized by progressive stiffness and weakness of the lower limbs. NGS stands for Next-Generation Sequencing, which is a high-throughput DNA sequencing technology that allows for the analysis of multiple genes simultaneously. The TFG SPG57 NGS genetic test is a diagnostic test that uses next-generation sequencing to analyze the TFG gene for any disease-causing mutations. This test can help confirm a diagnosis of SPG57 in individuals with suspected hereditary spastic paraplegia and can also be used for carrier testing in individuals with a family history of the condition. The results of the TFG SPG57 NGS genetic test can provide valuable information for genetic counseling, family planning, and potential treatment options. It is important to consult with a healthcare professional or genetic counselor to understand the implications and limitations of the test results. |