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. |