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TFG Gene SPG57 Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The TFG Gene SPG57 Genetic Test is a specialized diagnostic tool used to identify mutations in the TFG gene, which are associated with SPG57, a form of hereditary spastic paraplegia. This condition is characterized by progressive stiffness and weakness of the legs, resulting from the degeneration of nerve pathways responsible for transmitting signals from the brain to the spinal cord and then to the muscles.

DNA Labs UAE offers this genetic test to help in the diagnosis and management of SPG57. By analyzing a sample of the patient’s DNA, the test can detect specific genetic alterations in the TFG gene that are linked to the condition, providing crucial information for accurate diagnosis, treatment planning, and genetic counseling.

The cost of the TFG Gene SPG57 Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the sophisticated laboratory procedures and expert analysis required to identify the presence of the genetic mutation associated with SPG57. For patients and families affected by hereditary spastic paraplegia, this test represents a critical step towards understanding their condition and making informed health care decisions.

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  • This test is not intended for medical diagnosis or treatment
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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.