WDR48 Gene SPG60 WDR48 Related Genetic Test sale cost 4400 AED
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WDR48 Gene SPG60 WDR48 Related Genetic Test Cost

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

-21%

The WDR48 gene, associated with SPG60 (Spastic Paraplegia 60), plays a crucial role in various cellular processes, including the regulation of autophagy and endosomal trafficking. Mutations in the WDR48 gene can lead to SPG60, a form of hereditary spastic paraplegia characterized by progressive weakness and spasticity of the lower limbs. The condition may also present additional neurological symptoms depending on the severity and specific mutation involved.

To diagnose and understand the genetic basis of SPG60 in affected individuals, DNA Labs UAE offers a specialized genetic test targeting the WDR48 gene. This test is designed to identify mutations within the WDR48 gene that could be responsible for the condition, providing essential information for accurate diagnosis, management, and genetic counseling.

The cost of the WDR48 gene-related genetic test at DNA Labs UAE is 4400 AED. This comprehensive test is conducted in a state-of-the-art facility, ensuring high accuracy and reliability of the results. By opting for this test, patients and their families can gain valuable insights into the genetic underpinnings of SPG60, facilitating informed decisions regarding treatment options and lifestyle adjustments to better manage the condition.

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WDR48 Gene SPG60 WDR48 related Genetic Test

Introduction

The WDR48 gene is associated with a form of hereditary spastic paraplegia (HSP) known as SPG60. HSP is a group of rare genetic disorders characterized by progressive weakness and stiffness of the legs (paraplegia) due to the degeneration of the nerves controlling muscle movement. SPG60 is caused by mutations in the WDR48 gene, which is involved in the process of protein degradation within cells.

Test Details

NGS (Next-Generation Sequencing) genetic testing is a powerful tool used to identify mutations in genes associated with various genetic disorders, including SPG60. This type of testing involves sequencing the DNA of an individual to detect specific genetic variations or mutations in the WDR48 gene that may be responsible for the development of SPG60.

Benefits of the Test

NGS genetic testing for WDR48-related SPG60 can help in:

  • Confirming a clinical diagnosis
  • Identifying carriers of the disease
  • Providing genetic counseling to affected individuals and their families
  • Aiding in the development of personalized treatment approaches
  • Potential future therapies for SPG60

Pre-Test Information

Before undergoing the WDR48 Gene SPG60 WDR48 related NGS Genetic DNA Test, it is important to provide the following information:

  • Clinical history of the patient who is going for the test
  • A genetic counseling session to draw a pedigree chart of family members affected with WDR48 Gene SPG60, WDR48 related

Test Components and Price

The test components include:

  • 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

The cost of the WDR48 Gene SPG60 WDR48 related Genetic Test is 4400.0 AED.

Conclusion

Consulting with a healthcare professional or a genetic counselor is important to discuss the benefits, limitations, and implications of genetic testing before undergoing any genetic testing procedure. NGS genetic testing for WDR48-related SPG60 can provide valuable information for diagnosis, treatment, and genetic counseling.

Test Name WDR48 Gene SPG60 WDR48 related 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 WDR48 Gene SPG60, WDR48 related NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with WDR48 Gene SPG60, WDR48 related
Test Details

The WDR48 gene is associated with a form of hereditary spastic paraplegia (HSP) known as SPG60. HSP is a group of rare genetic disorders characterized by progressive weakness and stiffness of the legs (paraplegia) due to the degeneration of the nerves controlling muscle movement. SPG60 is caused by mutations in the WDR48 gene, which is involved in the process of protein degradation within cells.

NGS (Next-Generation Sequencing) genetic testing is a powerful tool used to identify mutations in genes associated with various genetic disorders, including SPG60. This type of testing involves sequencing the DNA of an individual to detect specific genetic variations or mutations in the WDR48 gene that may be responsible for the development of SPG60.

NGS genetic testing for WDR48-related SPG60 can help in confirming a clinical diagnosis, identifying carriers of the disease, and providing genetic counseling to affected individuals and their families. It can also aid in the development of personalized treatment approaches and potential future therapies for SPG60.

It is important to consult with a healthcare professional or a genetic counselor to discuss the benefits, limitations, and implications of genetic testing before undergoing any genetic testing procedure.

SKU: TEST-2025 Category:

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