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PRX Gene CMT4F Genetic Test Cost

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

-21%

The PRX Gene CMT4F Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the PRX gene, which are known to cause Charcot-Marie-Tooth disease type 4F (CMT4F). Charcot-Marie-Tooth disease is a group of inherited disorders that affect the peripheral nerves, leading to muscle weakness and sensory problems, primarily in the arms and legs. CMT4F is a rare subtype characterized by severe nerve damage and onset in childhood or adolescence.

This genetic test involves analyzing the patient’s DNA to search for specific alterations in the PRX gene that are indicative of CMT4F. Early detection through this test can be crucial for the management and treatment of the condition, allowing healthcare providers to tailor interventions that can help manage symptoms, improve quality of life, and provide genetic counseling for affected families.

The cost of the PRX Gene CMT4F Genetic Test at DNA Labs UAE is 4400 AED. The test is conducted in a state-of-the-art laboratory setting by professionals who specialize in genetic diagnostics. The process involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed using advanced genetic sequencing technologies to identify any mutations in the PRX gene.

Choosing DNA Labs UAE for this test ensures access to leading-edge technology, expert analysis, and comprehensive support throughout the testing process, making it a valuable resource for individuals and families seeking answers about Charcot-Marie-Tooth disease type 4F.

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  • 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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PRX Gene CMT4F Genetic Test

At DNA Labs UAE, we offer the PRX Gene CMT4F Genetic Test at a cost of AED 4400.0.

Test Details

The PRX gene is associated with Charcot-Marie-Tooth disease type 4F (CMT4F), a rare genetic disorder that affects the peripheral nerves. Our NGS genetic testing for the PRX gene can help diagnose CMT4F and provide information about the specific genetic mutations causing the disease. This information is crucial for treatment decisions and family 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

Pre Test Information

Before undergoing the PRX Gene CMT4F NGS Genetic DNA 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 PRX Gene CMT4F.

How the Test Works

The test involves sequencing the entire PRX gene to identify any mutations or variations that may contribute to the development of CMT4F. It is typically ordered by a healthcare provider and performed on a blood or saliva sample. Results are usually available within a few weeks and can be used to inform treatment decisions and genetic counseling.

Test Name PRX Gene CMT4F 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 PRX Gene CMT4F NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PRX Gene CMT4F
Test Details

The PRX gene is associated with Charcot-Marie-Tooth disease type 4F (CMT4F), which is a rare genetic disorder that affects the peripheral nerves. NGS genetic testing for the PRX gene can help diagnose CMT4F and provide information about the specific genetic mutations that are causing the disease. This can help guide treatment decisions and provide important information for family planning. The test involves sequencing the entire PRX gene to identify any mutations or variations that may be contributing to the development of CMT4F. It is typically ordered by a healthcare provider and performed on a blood or saliva sample. Results are typically available within a few weeks and can be used to inform treatment decisions and genetic counseling.

SKU: TEST-1191