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FA2H Gene SPG35 Genetic Test Cost

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

-21%

The FA2H gene SPG35 genetic test is a specialized diagnostic procedure aimed at detecting mutations in the FA2H gene, which are associated with a rare form of hereditary spastic paraplegia (HSP), known as SPG35. This condition is characterized by progressive weakness and stiffness of the legs, and in some cases, it may also affect the arms and other parts of the body. The genetic test is crucial for accurate diagnosis, enabling targeted management and genetic counseling for affected individuals and their families.

Conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing capabilities, the FA2H gene SPG35 genetic test involves analyzing the patient’s DNA to identify mutations in the FA2H gene. This gene plays a significant role in the metabolism of certain fats in the brain and nervous system, and mutations can lead to the neurological symptoms observed in SPG35.

The cost of the FA2H gene SPG35 genetic test at DNA Labs UAE is set at 4400 AED. This price reflects the sophisticated nature of the testing process, including the extraction of DNA, the use of advanced sequencing technologies to scrutinize the FA2H gene, and the expert analysis required to interpret the results accurately. While the cost may seem high, the test offers invaluable insights for affected individuals, guiding treatment options and helping families understand the risk of inheritance.

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  • This test is not intended for medical diagnosis or treatment
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FA2H Gene SPG35 Genetic Test

At DNA Labs UAE, we offer the FA2H Gene SPG35 Genetic Test for individuals who may be affected by hereditary spastic paraplegia (HSP). This test can help diagnose SPG35 and provide valuable information about the condition.

Test Components

The FA2H Gene SPG35 Genetic Test includes the following components:

  • 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

Test Cost

The cost of the FA2H Gene SPG35 Genetic Test is AED 4400.0.

Test Details

The FA2H gene, also known as the fatty acid 2-hydroxylase gene, is associated with a specific type of hereditary spastic paraplegia called SPG35. HSP is characterized by progressive weakness and stiffness of the legs due to degeneration of the nerve fibers that control muscle movement.

NGS (Next-Generation Sequencing) genetic testing is used to analyze multiple genes simultaneously. In the context of SPG35, NGS genetic testing can identify mutations or variations in the FA2H gene that may be responsible for the development of the condition.

NGS genetic testing can help confirm a diagnosis of SPG35, provide information about disease prognosis, inheritance patterns, and potential treatment options. It can also be used for carrier testing and prenatal diagnosis in families with a known FA2H gene mutation.

Before undergoing the FA2H SPG35 NGS genetic test, it is important to consult with a healthcare professional or genetic counselor to understand the benefits, limitations, and implications of the test.

Pre Test Information

Prior to the FA2H Gene SPG35 NGS Genetic DNA Test, it is recommended to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with FA2H Gene SPG35.

For more information or to schedule an appointment, please contact DNA Labs UAE.

Test Name FA2H Gene SPG35 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 FA2H Gene SPG35 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with FA2H Gene SPG35
Test Details

The FA2H gene, also known as the fatty acid 2-hydroxylase gene, is associated with a specific type of hereditary spastic paraplegia called SPG35. Hereditary spastic paraplegia (HSP) is a group of genetic disorders characterized by progressive weakness and stiffness of the legs (paraplegia) due to degeneration of the nerve fibers that control muscle movement.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of SPG35, NGS genetic testing can be used to identify mutations or variations in the FA2H gene that may be responsible for the development of the condition.

By identifying specific genetic changes in the FA2H gene, NGS genetic testing can help confirm a diagnosis of SPG35 and provide important information about disease prognosis, inheritance patterns, and potential treatment options. It can also be used for carrier testing and prenatal diagnosis in families with a known FA2H gene mutation.

It is important to consult with a healthcare professional or genetic counselor to understand the benefits, limitations, and implications of FA2H SPG35 NGS genetic testing before undergoing the test.

SKU: TEST-2003 Category:

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