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HSPB8 Gene CMT2L Genetic Test

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

-21%

The HSPB8 Gene CMT2L Genetic Test is a specific diagnostic tool used to identify mutations in the HSPB8 gene, which are associated with Charcot-Marie-Tooth disease type 2L (CMT2L). Charcot-Marie-Tooth disease is a group of hereditary disorders that affect the peripheral nerves, leading to muscle weakness and sensory problems, primarily in the feet and legs, and sometimes in the hands and arms. CMT2L is a subtype of this condition characterized by its genetic origin—the mutation in the HSPB8 gene.

This test is critical for individuals who have a family history of Charcot-Marie-Tooth disease or exhibit symptoms consistent with the condition. Early and accurate diagnosis through the HSPB8 Gene CMT2L Genetic Test can facilitate timely intervention, potential treatment options, and genetic counseling for affected individuals and their families.

The test is available at DNA Labs UAE, a reputable facility known for its comprehensive genetic testing services. The cost of the HSPB8 Gene CMT2L Genetic Test is 4400 AED. The testing process involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed in the laboratory for the presence of mutations in the HSPB8 gene. Results from this test can provide valuable information for the management and understanding of Charcot-Marie-Tooth disease type 2L.

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  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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HSPB8 Gene CMT2L Genetic Test

Welcome to DNA Labs UAE, where we offer the HSPB8 Gene CMT2L Genetic Test. This test helps identify mutations in the HSPB8 gene associated with Charcot-Marie-Tooth disease type 2L (CMT2L). CMT2L is a rare inherited peripheral neuropathy that affects the motor and sensory nerves in the arms and legs.

Test Details

The HSPB8 gene CMT2L NGS genetic test is a diagnostic test that uses Next Generation Sequencing (NGS) technology to analyze the DNA sequence of the HSPB8 gene. By identifying any mutations present, this test can help confirm a diagnosis of CMT2L and identify carriers of the mutation who may be at risk of passing it on to their children.

Components and Price

The cost of the HSPB8 Gene CMT2L Genetic Test is AED 4400.0. The test requires a blood sample or extracted DNA, or one drop of blood on an FTA Card. The report delivery time is approximately 3 to 4 weeks.

Method and Test Type

The HSPB8 Gene CMT2L Genetic Test utilizes NGS technology to analyze the DNA sequence of the HSPB8 gene. This test falls under the category of Neurological Disorders and is performed in our Genetics department.

Pre Test Information

Prior to undergoing the HSPB8 Gene CMT2L NGS Genetic DNA Test, it is recommended to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with HSPB8 Gene CMT2L. This information will assist in the interpretation of the test results.

Doctor and Test Department

The HSPB8 Gene CMT2L Genetic Test is performed by a Neurologist in our Genetics department.

Conclusion

The HSPB8 Gene CMT2L Genetic Test offered at DNA Labs UAE is a valuable diagnostic tool for identifying mutations in the HSPB8 gene associated with CMT2L. By providing this information, we can assist in confirming a diagnosis, identifying carriers, and offering genetic counseling to help families make informed decisions about their reproductive options.

Test Name HSPB8 Gene CMT2L 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 HSPB8 Gene CMT2L NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with HSPB8 Gene CMT2L
Test Details

HSPB8 gene CMT2L NGS genetic test is a diagnostic test that helps to identify mutations in the HSPB8 gene that are associated with Charcot-Marie-Tooth disease type 2L (CMT2L). CMT2L is a rare inherited peripheral neuropathy that affects the motor and sensory nerves in the arms and legs. This genetic test uses Next Generation Sequencing (NGS) technology to analyze the DNA sequence of the HSPB8 gene and identify any mutations that may be present. The test is performed on a blood sample and can help to confirm a diagnosis of CMT2L, as well as identify carriers of the mutation who may be at risk of passing it on to their children. This information can be used to provide genetic counseling and help families make informed decisions about their reproductive options.