CYLD Gene Trichoepithelioma multiple familial type 1 Genetic Test
Test Name: CYLD Gene Trichoepithelioma multiple familial type 1 Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
Price: 4400.0 AED
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 Trichoepithelioma, multiple familial, type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CYLD Gene Trichoepithelioma, multiple familial, type 1 NGS Genetic DNA Test gene CYLD
Test Details: CYLD gene trichoepithelioma, multiple familial, type 1 (CYLD-TMF1) is a rare genetic disorder characterized by the development of multiple benign skin tumors called trichoepitheliomas. These tumors typically occur on the face and can be present from early childhood or adolescence. A NGS (Next-Generation Sequencing) genetic test can be used to identify mutations in the CYLD gene, which is associated with CYLD-TMF1. This test involves sequencing the DNA of an individual to detect any genetic alterations or mutations in the CYLD gene. The NGS genetic test for CYLD-TMF1 can help confirm a diagnosis in individuals suspected to have this condition. It can also be used for genetic counseling and to identify at-risk family members who may carry the CYLD gene mutation. It is important to note that a positive genetic test result does not necessarily mean that an individual will develop trichoepitheliomas or other symptoms associated with CYLD-TMF1. The severity and specific features of the condition can vary widely among affected individuals, even within the same family. If you suspect that you or a family member may have CYLD-TMF1, it is recommended to consult with a healthcare professional or a genetic counselor who can provide further information and guidance regarding genetic testing options and management of the condition.
Test Name | CYLD Gene Trichoepithelioma multiple familial type 1 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 Trichoepithelioma, multiple familial, type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CYLD Gene Trichoepithelioma, multiple familial, type 1 NGS Genetic DNA Test gene CYLD |
Test Details |
CYLD gene trichoepithelioma, multiple familial, type 1 (CYLD-TMF1) is a rare genetic disorder characterized by the development of multiple benign skin tumors called trichoepitheliomas. These tumors typically occur on the face and can be present from early childhood or adolescence. A NGS (Next-Generation Sequencing) genetic test can be used to identify mutations in the CYLD gene, which is associated with CYLD-TMF1. This test involves sequencing the DNA of an individual to detect any genetic alterations or mutations in the CYLD gene. The NGS genetic test for CYLD-TMF1 can help confirm a diagnosis in individuals suspected to have this condition. It can also be used for genetic counseling and to identify at-risk family members who may carry the CYLD gene mutation. It is important to note that a positive genetic test result does not necessarily mean that an individual will develop trichoepitheliomas or other symptoms associated with CYLD-TMF1. The severity and specific features of the condition can vary widely among affected individuals, even within the same family. If you suspect that you or a family member may have CYLD-TMF1, it is recommended to consult with a healthcare professional or a genetic counselor who can provide further information and guidance regarding genetic testing options and management of the condition. |