Sale!

CYLD Gene Trichoepithelioma Multiple Familial Type 1 Genetic Test Cost

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

-21%

The CYLD Gene Trichoepithelioma Multiple Familial Type 1 Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the CYLD gene, which are linked to the development of Trichoepithelioma Multiple Familial Type 1. This condition is a rare genetic disorder characterized by the appearance of multiple benign skin tumors, primarily affecting the face, scalp, and neck. These tumors, known as trichoepitheliomas, typically begin to develop in late childhood or adolescence.

This genetic test is crucial for families with a history of this condition, as it allows for the early identification of affected individuals. Early diagnosis can lead to timely intervention and management of the condition, potentially reducing the physical and psychological impact of the skin tumors. The test involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the laboratory for mutations in the CYLD gene.

The cost of the CYLD Gene Trichoepithelioma Multiple Familial Type 1 Genetic Test at DNA Labs UAE is 4400 AED. This cost reflects the specialized nature of the test and the comprehensive analysis required to accurately identify the genetic mutation. For individuals with a family history of Trichoepithelioma Multiple Familial Type 1, this test provides a valuable resource for genetic counseling and planning for future healthcare needs.

Description

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.