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CYLD Gene Spiegler-Brooke Syndrome Genetic Test Cost

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

-21%

The CYLD gene Spiegler-Brooke Syndrome genetic test is a specialized diagnostic procedure aimed at identifying mutations in the CYLD gene, which are linked to the development of Spiegler-Brooke Syndrome. This rare condition is characterized by the growth of multiple benign skin tumors that typically appear in adolescence or early adulthood. These tumors can vary in size and are often found on the scalp, face, and trunk. The syndrome can also lead to tumors in other parts of the body, including internal organs.

The test is performed by collecting a DNA sample, usually through a blood draw or cheek swab, and analyzing it for specific mutations in the CYLD gene. Identifying these mutations can confirm a diagnosis of Spiegler-Brooke Syndrome, which is crucial for managing the condition and planning appropriate treatment. Early diagnosis can help in monitoring and potentially removing tumors before they cause discomfort or lead to complications.

This genetic test is available at DNA Labs UAE, a leading facility in genetic testing and analysis. The cost of the test is 4400 AED, which reflects the comprehensive analysis and expertise required to accurately identify mutations in the CYLD gene. By opting for this test at DNA Labs UAE, patients can expect reliable results, professional counseling, and guidance on the implications of the test outcomes for their health and management of the syndrome.

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CYLD Gene Spiegler-Brooke syndrome Genetic Test

Cost: AED 4400.0

Components:

  • Test Name: CYLD Gene Spiegler-Brooke syndrome Genetic Test
  • Price: AED 4400.0
  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Method: NGS Technology
  • Test Type: Cancer
  • Doctor: Oncologist
  • Test Department: Genetics
  • Pre Test Information: Clinical History of Patient who is going for CYLD Gene Spiegler-Brooke syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CYLD Gene Spiegler-Brooke syndrome NGS Genetic DNA Test gene CYLD

Test Details

The CYLD gene is associated with a condition called CYLD syndrome, also known as Brooke-Spiegler syndrome. This syndrome is a rare genetic disorder that affects the skin appendages, such as hair follicles, sweat glands, and sebaceous glands.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. It allows for a more comprehensive analysis of the patient’s DNA, providing a faster and more accurate diagnosis.

In the case of CYLD syndrome, NGS genetic testing can be used to identify mutations or changes in the CYLD gene that may be responsible for the condition. This can help confirm a diagnosis, guide treatment decisions, and provide information about the risk of passing the condition on to future generations.

It is important to note that genetic testing should be conducted and interpreted by a qualified healthcare professional, such as a geneticist or genetic counselor, who can provide appropriate counseling and support.

Test Name CYLD Gene Spiegler-Brooke syndrome Genetic Test
Components
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 Cancer
Doctor Oncologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for CYLD Gene Spiegler-Brooke syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CYLD Gene Spiegler-Brooke syndrome NGS Genetic DNA Test gene CYLD
Test Details

The CYLD gene is associated with a condition called CYLD syndrome, also known as Brooke-Spiegler syndrome. This syndrome is a rare genetic disorder that affects the skin appendages, such as hair follicles, sweat glands, and sebaceous glands.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. It allows for a more comprehensive analysis of the patient’s DNA, providing a faster and more accurate diagnosis.

In the case of CYLD syndrome, NGS genetic testing can be used to identify mutations or changes in the CYLD gene that may be responsible for the condition. This can help confirm a diagnosis, guide treatment decisions, and provide information about the risk of passing the condition on to future generations.

It is important to note that genetic testing should be conducted and interpreted by a qualified healthcare professional, such as a geneticist or genetic counselor, who can provide appropriate counseling and support.

SKU: TEST-4579 Category:

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