RB1 Gene Hereditary Retinoblastoma Genetic Test
Welcome to DNA Labs UAE, where we offer the RB1 Gene Hereditary Retinoblastoma Genetic Test. This test is designed to analyze the RB1 gene, which is associated with the development of retinoblastoma, a rare type of eye cancer that primarily affects young children.
- 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: Ophthalmology Disorders
- Doctor: Ophthalmologist
- Test Department: Genetics
Pre Test Information
Prior to undergoing the RB1 Gene Hereditary Retinoblastoma Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by RB1 Gene Hereditary Retinoblastoma.
Hereditary retinoblastoma is caused by mutations in the RB1 gene that are inherited from a parent. Our NGS genetic testing utilizes next-generation sequencing technology to analyze multiple genes simultaneously, allowing for a comprehensive evaluation of genetic mutations associated with hereditary retinoblastoma.
The RB1 gene and other genes associated with the condition will be analyzed during the test. Samples can be obtained through blood or saliva, and results are typically available within a few weeks.
Genetic testing for hereditary retinoblastoma can provide valuable information regarding an individual’s risk of developing the condition, as well as guide appropriate screening and management strategies. We understand the significance of these results and offer counseling and support to individuals and families throughout the testing process.
|RB1 Gene Hereditary Retinoblastoma Genetic Test
|Blood or Extracted DNA or One drop Blood on FTA Card
|3 to 4 Weeks
|Pre Test Information
|Clinical History of Patient who is going for RB1 Gene Hereditary Retinoblastoma NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RB1 Gene Hereditary Retinoblastoma NGS Genetic DNA Test gene RB1
The RB1 gene is a tumor suppressor gene that is associated with the development of retinoblastoma, a rare type of eye cancer that typically affects young children. Hereditary retinoblastoma is caused by mutations in the RB1 gene that are passed down from a parent to their child.
NGS (next-generation sequencing) genetic testing is a type of DNA sequencing that can analyze multiple genes at once, allowing for a comprehensive evaluation of genetic mutations that may be associated with a particular condition, such as hereditary retinoblastoma. This type of testing can help identify individuals who are at increased risk of developing retinoblastoma and inform appropriate screening and management strategies.
NGS genetic testing for hereditary retinoblastoma typically involves analyzing the RB1 gene and other genes that may be associated with the condition. The test is usually performed on a blood or saliva sample, and results are typically available within a few weeks. Counseling and support are typically provided to individuals and families who undergo genetic testing, as the results can have important implications for their health and well-being.