REEP1 Gene SPG31 Genetic Test sale cost 4400 AED
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REEP1 Gene SPG31 Genetic Test Cost

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

-21%

The REEP1 gene SPG31 genetic test is a specialized diagnostic tool aimed at detecting mutations in the REEP1 gene, which are associated with Spastic Paraplegia 31 (SPG31). SPG31 is a form of hereditary spastic paraplegia, a group of genetic disorders characterized by progressive stiffness and weakness of the legs. Mutations in the REEP1 gene disrupt the normal function of neurons in the spinal cord, leading to the symptoms associated with the condition.

The test is conducted by DNA Labs UAE, a reputable facility known for its comprehensive range of genetic testing services. By analyzing a sample of the patient’s DNA, the test can identify specific mutations in the REEP1 gene that are linked to SPG31. This information is crucial for accurate diagnosis, enabling healthcare providers to offer appropriate genetic counseling and tailor management strategies to the individual’s needs.

The cost of the REEP1 gene SPG31 genetic test at DNA Labs UAE is 4400 AED. This price reflects the sophisticated technology and expertise required to accurately identify mutations in the REEP1 gene. For patients and families affected by hereditary spastic paraplegia, this test represents a critical step towards understanding their condition and making informed decisions about their care.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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REEP1 Gene SPG31 Genetic Test

At DNA Labs UAE, we offer the REEP1 Gene SPG31 Genetic Test to diagnose hereditary spastic paraplegia (HSP) associated with the REEP1 gene. HSP is characterized by progressive weakness and stiffness in the legs, making it difficult to walk.

Test Details

The REEP1 gene is analyzed using Next-Generation Sequencing (NGS) technology, which allows for the simultaneous analysis of multiple genes. This comprehensive evaluation of a person’s genetic makeup helps identify mutations or variations in the REEP1 gene that may be causing SPG31.

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: Neurological Disorders
  • Doctor: Neurologist
  • Test Department: Genetics

Pre Test Information

Prior to the REEP1 Gene SPG31 Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by SPG31.

Importance of NGS Genetic Testing

NGS genetic testing offers a comprehensive analysis of a person’s genetic makeup, allowing healthcare professionals to confirm a diagnosis of SPG31 by identifying mutations in the REEP1 gene. This information is valuable for genetic counseling, family planning, and potentially identifying targeted treatment options in the future.

Please note that NGS genetic testing may not be available in all healthcare settings. It should be performed by qualified professionals trained in genetic analysis and interpretation. It is crucial to discuss genetic testing results with a healthcare provider or genetic counselor to fully understand their implications and potential impact on an individual’s health.

Test Name REEP1 Gene SPG31 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 REEP1 Gene SPG31 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with REEP1 Gene SPG31
Test Details

The REEP1 gene is associated with a type of hereditary spastic paraplegia called SPG31. Hereditary spastic paraplegia (HSP) is a group of genetic disorders characterized by progressive weakness and stiffness in the legs, leading to difficulty walking.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, providing a comprehensive evaluation of a person’s genetic makeup. In the case of SPG31, NGS genetic testing can be used to identify mutations or variations in the REEP1 gene that may be causing the condition.

By analyzing the REEP1 gene through NGS, healthcare professionals can determine if a person has a mutation in this gene, which can help confirm a diagnosis of SPG31. This information can also be useful in genetic counseling, family planning, and potentially identifying targeted treatment options in the future.

It’s important to note that NGS genetic testing may not be available in all healthcare settings and should be performed by qualified professionals trained in genetic analysis and interpretation. Additionally, genetic testing results should always be discussed with a healthcare provider or genetic counselor to fully understand their implications and potential impact on an individual’s health.

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