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PRPS1 Gene CMTX5 Genetic Test Cost

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

-21%

The PRPS1 Gene CMTX5 Genetic Test is a specialized diagnostic tool designed to identify mutations in the PRPS1 gene, which are linked to Charcot-Marie-Tooth disease, type X5 (CMTX5). CMTX5 is a rare form of Charcot-Marie-Tooth disease, a genetic disorder that affects the peripheral nerves, leading to muscle weakness and sensory problems. The PRPS1 gene plays a crucial role in the synthesis of nucleotides, which are essential for DNA and RNA production. Mutations in this gene can disrupt nerve function, resulting in the symptoms associated with CMTX5.

This genetic test is available at DNA Labs UAE, a leading facility for genetic testing and analysis. The test is performed through a blood sample or a cheek swab, which is then analyzed for specific genetic alterations in the PRPS1 gene. The outcome of this test can provide valuable information for the diagnosis, treatment, and management of CMTX5, offering insights into potential therapeutic approaches and enabling families to understand their genetic risk for this condition.

The cost of the PRPS1 Gene CMTX5 Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to accurately detect mutations in the PRPS1 gene, providing patients and healthcare providers with critical information for managing Charcot-Marie-Tooth disease, type X5.

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  • This test is not intended for medical diagnosis or treatment
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PRPS1 Gene CMTX5 Genetic Test

At DNA Labs UAE, we offer the PRPS1 Gene CMTX5 Genetic Test to help diagnose and manage Charcot-Marie-Tooth disease type X5 (CMTX5). This rare inherited disorder affects the peripheral nerves and can have a significant impact on an individual’s quality of life.

Test Details

The PRPS1 gene is analyzed using Next-Generation Sequencing (NGS) technology to identify any mutations that may be causing CMTX5. This information is crucial for accurate diagnosis and treatment planning.

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

Symptoms and Diagnosis

CMTX5 presents with various symptoms, including weakness and wasting of the muscles in the feet and lower legs, difficulty walking, and decreased sensation in the limbs. A thorough clinical history of the patient is essential for accurate diagnosis. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by CMTX5.

Importance of the Test

The PRPS1 Gene CMTX5 Genetic Test is crucial for several reasons. Firstly, it can confirm a diagnosis of CMTX5 and provide information about the risk of passing the disease on to future generations. This knowledge is vital for family planning and making informed decisions about reproduction. Secondly, the test results can help guide treatment and management strategies for individuals with CMTX5, improving their quality of life.

Conclusion

The PRPS1 Gene CMTX5 Genetic Test offered by DNA Labs UAE is a valuable tool for diagnosing and managing Charcot-Marie-Tooth disease type X5. With its accurate results and comprehensive analysis, this test provides crucial information for patients, their families, and healthcare professionals. Early diagnosis and proper management can greatly improve the prognosis and quality of life for individuals affected by CMTX5.

Test Name PRPS1 Gene CMTX5 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 PRPS1 Gene CMTX5 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PRPS1 Gene CMTX5
Test Details

The PRPS1 gene is associated with Charcot-Marie-Tooth disease type X5 (CMTX5), which is a rare inherited disorder that affects the peripheral nerves. The NGS genetic test for CMTX5 analyzes the PRPS1 gene for mutations that can cause the disease. This test can help diagnose CMTX5 and provide information about the risk of passing the disease on to future generations. It can also help guide treatment and management strategies for individuals with CMTX5.

SKU: TEST-1199 Category:

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