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PMP22 Gene Dejerine-Sottas Disease Genetic Test Cost

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

-21%

The PMP22 Gene Dejerine-Sottas Disease Genetic Test is a specialized diagnostic tool used to detect mutations in the PMP22 gene, which are associated with Dejerine-Sottas Disease, also known as hereditary motor and sensory neuropathy type III. This condition is a type of Charcot-Marie-Tooth disease, characterized by severe neurological symptoms that include muscle weakness, sensory loss, and in some cases, deformities in the extremities due to nerve damage.

DNA Labs UAE offers this genetic test to individuals who exhibit symptoms of Dejerine-Sottas Disease or have a family history of the condition. The test involves collecting a DNA sample, usually through a blood draw, which is then analyzed in the lab to identify any mutations in the PMP22 gene.

The cost of the PMP22 Gene Dejerine-Sottas Disease Genetic Test at DNA Labs UAE is 4400 AED. This price may cover the test procedure, analysis, and a comprehensive report that explains the results. It’s important for patients to consult with a healthcare provider or a genetic counselor before and after taking the test to understand the implications of the results and to discuss potential treatment options or management strategies for the condition.

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PMP22 Gene Dejerine-Sottas disease Genetic Test

Cost: 4400.0 AED

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 PMP22 Gene Dejerine-Sottas disease NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PMP22 Gene Dejerine-Sottas disease.

Test Details:

The PMP22 gene is associated with Dejerine-Sottas disease, a rare genetic disorder that affects the peripheral nerves. The disease is characterized by muscle weakness, decreased sensation, and impaired reflexes.

NGS (next-generation sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. This type of testing can identify mutations or variations in the PMP22 gene that may be associated with Dejerine-Sottas disease.

NGS genetic testing is a valuable tool for diagnosing genetic disorders, including Dejerine-Sottas disease. It can also help identify carriers of the disease and provide information for family planning and genetic counseling.

Test Name PMP22 Gene Dejerine-Sottas disease 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 PMP22 Gene Dejerine-Sottas disease NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PMP22 Gene Dejerine-Sottas disease
Test Details

The PMP22 gene is associated with Dejerine-Sottas disease, a rare genetic disorder that affects the peripheral nerves. The disease is characterized by muscle weakness, decreased sensation, and impaired reflexes.

NGS (next-generation sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. This type of testing can identify mutations or variations in the PMP22 gene that may be associated with Dejerine-Sottas disease.

NGS genetic testing is a valuable tool for diagnosing genetic disorders, including Dejerine-Sottas disease. It can also help identify carriers of the disease and provide information for family planning and genetic counseling.

SKU: TEST-1230 Category:

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