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MPZ Gene DI-CMTD Genetic Test

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

-21%

The MPZ Gene DI-CMTD Genetic Test is a specialized diagnostic tool designed to identify mutations in the MPZ gene, which are associated with a subtype of Charcot-Marie-Tooth disease known as Dominant Intermediate Charcot-Marie-Tooth Disease Type D (DI-CMTD). 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 feet and legs, and sometimes the hands and arms.

The MPZ gene plays a crucial role in the functioning and maintenance of the myelin sheath, a protective layer that surrounds nerve fibers. Mutations in this gene can disrupt the normal function of peripheral nerves, leading to the symptoms observed in DI-CMTD. Early and accurate diagnosis through the MPZ Gene DI-CMTD Genetic Test can be critical for the management and treatment of the condition, allowing for targeted therapies and interventions that can improve quality of life.

This genetic test is offered by DNA Labs UAE, a reputable facility known for its advanced diagnostic services. The test is priced at 4400 AED, reflecting the specialized nature of the analysis and the sophisticated technology employed to ensure accurate results. For individuals displaying symptoms of Charcot-Marie-Tooth disease or those with a family history of the condition, the MPZ Gene DI-CMTD Genetic Test can provide essential insights into their genetic makeup, guiding both patients and healthcare providers in making informed decisions about management and treatment strategies.

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  • This test is not intended for medical diagnosis or treatment
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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.