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MTMR2 Gene CMT4B1 Genetic Test

4,400 د.إ

-21%

The MTMR2 gene CMT4B1 genetic test is a specialized diagnostic tool used to detect mutations in the MTMR2 gene, which are associated with Charcot-Marie-Tooth disease type 4B1 (CMT4B1). This condition is a rare, inherited, neurological disorder characterized by the degeneration of peripheral nerves, leading to muscle weakness and sensory loss, typically starting in the limbs. The test involves analyzing the patient’s DNA to identify any genetic alterations in the MTMR2 gene that may indicate the presence of CMT4B1.

This genetic test is crucial for individuals who exhibit symptoms suggestive of Charcot-Marie-Tooth disease or have a family history of the condition, as it helps in confirming the diagnosis, understanding the disease progression, and making informed decisions about management and treatment options. Early diagnosis through genetic testing can significantly improve the quality of life for affected individuals by facilitating timely interventions and support.

The MTMR2 gene CMT4B1 genetic test is available at DNA Labs UAE, a leading facility in genetic testing and analysis. The cost of the test is 4400 AED, reflecting the specialized nature of the analysis and the expertise required to accurately interpret the results. By choosing DNA Labs UAE for this test, patients can expect high-quality services, accurate results, and comprehensive support throughout the testing process.

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MTMR2 Gene CMT4B1 Genetic Test

Test Name: MTMR2 Gene CMT4B1 Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

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: Clinical History of Patient who is going for MTMR2 Gene CMT4B1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MTMR2 Gene CMT4B1.

Test Details

The MTMR2 gene is associated with Charcot-Marie-Tooth disease type 4B1 (CMT4B1), which is a rare genetic disorder that affects the peripheral nerves. CMT4B1 is caused by mutations in the MTMR2 gene, which provides instructions for making a protein that is involved in the breakdown of certain lipids in cells.

NGS genetic testing for CMT4B1 involves analyzing the DNA sequence of the MTMR2 gene to identify any mutations that may be causing the disease. This type of testing can help diagnose CMT4B1 and provide information about the specific genetic changes that are responsible for the disorder.

NGS genetic testing for CMT4B1 may be recommended for individuals who have symptoms of the disorder, a family history of CMT, or who have been previously diagnosed with another type of CMT and are not responding to treatment. Testing may also be recommended for individuals who are considering having children and want to know their risk of passing on the disorder to their offspring.

If a mutation is identified through NGS genetic testing for CMT4B1, genetic counseling may be recommended to help individuals and their families understand the implications of the diagnosis and make informed decisions about treatment and family planning.

Test Name MTMR2 Gene CMT4B1 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 MTMR2 Gene CMT4B1 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MTMR2 Gene CMT4B1
Test Details

The MTMR2 gene is associated with Charcot-Marie-Tooth disease type 4B1 (CMT4B1), which is a rare genetic disorder that affects the peripheral nerves. CMT4B1 is caused by mutations in the MTMR2 gene, which provides instructions for making a protein that is involved in the breakdown of certain lipids in cells.

NGS genetic testing for CMT4B1 involves analyzing the DNA sequence of the MTMR2 gene to identify any mutations that may be causing the disease. This type of testing can help diagnose CMT4B1 and provide information about the specific genetic changes that are responsible for the disorder.

NGS genetic testing for CMT4B1 may be recommended for individuals who have symptoms of the disorder, a family history of CMT, or who have been previously diagnosed with another type of CMT and are not responding to treatment. Testing may also be recommended for individuals who are considering having children and want to know their risk of passing on the disorder to their offspring.

If a mutation is identified through NGS genetic testing for CMT4B1, genetic counseling may be recommended to help individuals and their families understand the implications of the diagnosis and make informed decisions about treatment and family planning.