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CYLD Gene Cylindromatosis Familial Genetic Test Cost

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

-21%

The “CYLD Gene Cylindromatosis Familial Genetic Test” is a specialized diagnostic procedure aimed at detecting mutations in the CYLD gene, which is known to cause cylindromatosis. Cylindromatosis is a rare genetic condition characterized by the development of multiple benign tumors, primarily affecting the skin. These tumors, known as cylindromas, typically arise in areas such as the scalp, face, and neck. The condition is inherited in an autosomal dominant pattern, meaning a single copy of the altered gene in each cell is sufficient to cause the disorder.

This genetic test is crucial for families with a history of cylindromatosis, as it helps in identifying individuals who carry the genetic mutation. Early identification of carriers allows for timely surveillance and management of the condition, potentially preventing or minimizing the development of skin tumors. Moreover, the test can provide essential information for affected families regarding the risk of passing the condition to future generations.

Conducted at DNA Labs UAE, the test involves collecting a DNA sample, typically through a blood draw or a cheek swab. The laboratory then analyzes the CYLD gene for specific mutations known to cause cylindromatosis. The cost of the test is 4400 AED, reflecting the specialized nature of the genetic analysis and the expertise required to interpret the results accurately.

Given the rarity of cylindromatosis and the importance of genetic counseling, individuals considering this test are often advised to consult with a genetic counselor or a specialist in genetic diseases. This professional guidance ensures that individuals and families fully understand the implications of the test results and the condition itself.

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CYLD Gene Cylindromatosis familial Genetic Test

Test Name: CYLD Gene Cylindromatosis familial 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 Cylindromatosis, familial NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CYLD Gene Cylindromatosis, familial NGS Genetic DNA Test gene CYLD

Test Details

CYLD gene, also known as cylindromatosis gene, is a gene that is associated with a condition called familial cylindromatosis. This condition is characterized by the development of multiple skin tumors known as cylindromas.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of familial cylindromatosis, NGS genetic testing can be used to analyze the CYLD gene for any mutations or variations that may be associated with the condition.

NGS genetic testing for CYLD gene mutations can help in diagnosing familial cylindromatosis and identifying individuals who are at risk of developing the condition. It can also be used for genetic counseling and to guide appropriate medical management and surveillance for affected individuals and their family members.

It is important to note that genetic testing for familial cylindromatosis should be done under the guidance of a healthcare professional or a genetic counselor who can provide appropriate pre- and post-test counseling and interpretation of the results.

Test Name CYLD Gene Cylindromatosis familial 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 Cylindromatosis, familial NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CYLD Gene Cylindromatosis, familial NGS Genetic DNA Test gene CYLD
Test Details

CYLD gene, also known as cylindromatosis gene, is a gene that is associated with a condition called familial cylindromatosis. This condition is characterized by the development of multiple skin tumors known as cylindromas.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of familial cylindromatosis, NGS genetic testing can be used to analyze the CYLD gene for any mutations or variations that may be associated with the condition.

NGS genetic testing for CYLD gene mutations can help in diagnosing familial cylindromatosis and identifying individuals who are at risk of developing the condition. It can also be used for genetic counseling and to guide appropriate medical management and surveillance for affected individuals and their family members.

It is important to note that genetic testing for familial cylindromatosis should be done under the guidance of a healthcare professional or a genetic counselor who can provide appropriate pre- and post-test counseling and interpretation of the results.