MPZ Gene DI-CMTD Genetic Test
Cost: 4400.0 AED
Test Details:
The MPZ gene is associated with a type of inherited peripheral neuropathy called Charcot-Marie-Tooth disease (CMT). DI-CMTD NGS genetic testing is a type of genetic test that uses next-generation sequencing (NGS) technology to identify mutations in the MPZ gene that may cause CMT.
CMT is a group of inherited disorders that affect the peripheral nerves, which are the nerves that connect the brain and spinal cord to the muscles and sensory organs. Symptoms of CMT can include muscle weakness and wasting, difficulty walking, foot deformities, and numbness or tingling in the hands and feet.
DI-CMTD NGS genetic testing can help diagnose CMT and identify the specific genetic mutation causing the disease. This information can be useful for making treatment decisions and providing genetic counseling to affected individuals and their families.
Test Components:
- 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:
Clinical History of Patient who is going for MPZ Gene DI-CMTD NGS Genetic DNA Test
A Genetic Counselling session to draw a pedigree chart of family members affected with MPZ Gene DI-CMTD
Test Name | MPZ Gene DI-CMTD 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 MPZ Gene DI-CMTD NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MPZ Gene DI-CMTD |
Test Details |
The MPZ gene is associated with a type of inherited peripheral neuropathy called Charcot-Marie-Tooth disease (CMT). DI-CMTD NGS genetic testing is a type of genetic test that uses next-generation sequencing (NGS) technology to identify mutations in the MPZ gene that may cause CMT. CMT is a group of inherited disorders that affect the peripheral nerves, which are the nerves that connect the brain and spinal cord to the muscles and sensory organs. Symptoms of CMT can include muscle weakness and wasting, difficulty walking, foot deformities, and numbness or tingling in the hands and feet. DI-CMTD NGS genetic testing can help diagnose CMT and identify the specific genetic mutation causing the disease. This information can be useful for making treatment decisions and providing genetic counseling to affected individuals and their families. |