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HSPB1 Gene CMT2F Genetic Test

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

-21%

The HSPB1 gene CMT2F genetic test is a specialized diagnostic tool aimed at identifying mutations in the HSPB1 gene, which are linked to Charcot-Marie-Tooth disease type 2F (CMT2F). Charcot-Marie-Tooth disease is a group of inherited disorders that affect the peripheral nerves, leading to muscle weakness and sensory problems, predominantly in the feet and legs. CMT2F is a specific subtype characterized by late-onset and predominantly affects motor nerves, though sensory nerves can also be involved.

The test involves analyzing the patient’s DNA, extracted from a blood sample, to look for specific genetic alterations in the HSPB1 gene that are known to cause CMT2F. Identifying these mutations can confirm a diagnosis of CMT2F, which is crucial for managing the disease, understanding its progression, and providing appropriate genetic counseling for affected families.

The test is offered by DNA Labs UAE, a leading facility in genetic testing and analysis in the United Arab Emirates. The cost of the HSPB1 gene CMT2F genetic test is 4400 AED. This price reflects the comprehensive nature of the test, including the sophisticated technology and expertise required to accurately identify mutations in the HSPB1 gene. By opting for this test at DNA Labs UAE, patients and their families can expect reliable results, professional genetic counseling, and guidance on the next steps following a diagnosis.

Home  Sample collection service available

  • 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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HSPB1 Gene CMT2F Genetic Test

Test Name: HSPB1 Gene CMT2F 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 HSPB1 Gene CMT2F NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with HSPB1 Gene CMT2F.

Test Details: The HSPB1 gene is associated with Charcot-Marie-Tooth disease type 2F (CMT2F), which is a rare genetic disorder that affects the peripheral nerves and causes muscle weakness and atrophy. The NGS genetic test for CMT2F analyzes the HSPB1 gene for mutations that can cause the disease. This test is useful for individuals who have symptoms of CMT2F or have a family history of the disease. Early diagnosis can help with the management of symptoms and treatment options. The test is performed using next-generation sequencing (NGS) technology, which can analyze multiple genes simultaneously and provide accurate results. Genetic counseling is recommended before and after the test to discuss the implications of the results and the risk of passing the mutation to future generations.

Test Name HSPB1 Gene CMT2F 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 HSPB1 Gene CMT2F NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with HSPB1 Gene CMT2F
Test Details

The HSPB1 gene is associated with Charcot-Marie-Tooth disease type 2F (CMT2F), which is a rare genetic disorder that affects the peripheral nerves and causes muscle weakness and atrophy. The NGS genetic test for CMT2F analyzes the HSPB1 gene for mutations that can cause the disease. This test is useful for individuals who have symptoms of CMT2F or have a family history of the disease. Early diagnosis can help with the management of symptoms and treatment options. The test is performed using next-generation sequencing (NGS) technology, which can analyze multiple genes simultaneously and provide accurate results. Genetic counseling is recommended before and after the test to discuss the implications of the results and the risk of passing the mutation to future generations.