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SBF2 Gene CMT4B2 Genetic Test

4,400 د.إ

-21%

The “SBF2 Gene CMT4B2 Genetic Test” is a specific diagnostic procedure aimed at detecting mutations in the SBF2 gene, which are responsible for Charcot-Marie-Tooth disease type 4B2 (CMT4B2). Charcot-Marie-Tooth disease is a group of inherited disorders that affect the peripheral nerves, leading to muscle weakness and atrophy, as well as sensory problems. The SBF2 gene plays a crucial role in the development and maintenance of myelin, the protective sheath surrounding nerve fibers. Mutations in this gene disrupt myelin integrity, impairing nerve function and leading to the symptoms associated with CMT4B2.

This genetic test is a vital tool for diagnosing CMT4B2, allowing for precise genetic counseling and aiding in the development of targeted treatment plans for affected individuals. The test involves collecting a DNA sample, typically through a blood draw, which is then analyzed in a laboratory setting to identify mutations in the SBF2 gene.

The cost of the “SBF2 Gene CMT4B2 Genetic Test” is 4400 AED. It is available at DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates. DNA Labs UAE is equipped with state-of-the-art technology and staffed by experienced professionals, ensuring accurate and reliable test results. This test is an important resource for individuals with a family history of Charcot-Marie-Tooth disease, offering them crucial information about their genetic health and helping guide their healthcare decisions.

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SBF2 Gene CMT4B2 Genetic Test

Test Name: SBF2 Gene CMT4B2 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 SBF2 Gene CMT4B2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SBF2 Gene CMT4B2.

Test Details: The SBF2 gene is associated with Charcot-Marie-Tooth disease type 4B2 (CMT4B2), which is a rare inherited neurological disorder that affects the peripheral nerves. CMT4B2 is caused by mutations in the SBF2 gene, which provides instructions for making a protein that is important for maintaining the structure and function of nerve cells.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that can analyze multiple genes at once, using advanced sequencing technology. This can be particularly useful for identifying mutations in genes that are associated with rare diseases like CMT4B2.

A genetic test for CMT4B2 may involve sequencing the SBF2 gene using NGS technology, to look for any mutations or changes in the DNA sequence that could be causing the disease. This information can be used to confirm a diagnosis of CMT4B2, and to provide information about the likely course of the disease and potential treatment options.

Test Name SBF2 Gene CMT4B2 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 SBF2 Gene CMT4B2 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SBF2 Gene CMT4B2
Test Details

The SBF2 gene is associated with Charcot-Marie-Tooth disease type 4B2 (CMT4B2), which is a rare inherited neurological disorder that affects the peripheral nerves. CMT4B2 is caused by mutations in the SBF2 gene, which provides instructions for making a protein that is important for maintaining the structure and function of nerve cells.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that can analyze multiple genes at once, using advanced sequencing technology. This can be particularly useful for identifying mutations in genes that are associated with rare diseases like CMT4B2.

A genetic test for CMT4B2 may involve sequencing the SBF2 gene using NGS technology, to look for any mutations or changes in the DNA sequence that could be causing the disease. This information can be used to confirm a diagnosis of CMT4B2, and to provide information about the likely course of the disease and potential treatment options.

SKU: TEST-1186 Category:

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