CYP1B1 Gene Glaucoma primary type 3A Genetic Test
Cost: AED 4400.0
Components:
- 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:
Clinical History of Patient who is going for CYP1B1 Gene Glaucoma, primary type 3A NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CYP1B1 Gene Glaucoma, primary type 3A NGS Genetic DNA Test gene CYP1B1.
Test Details:
The CYP1B1 gene is associated with primary type 3A glaucoma, a rare form of glaucoma that typically affects infants and young children. This condition is characterized by high intraocular pressure, optic nerve damage, and visual impairment.
NGS genetic testing for the CYP1B1 gene can identify mutations or variations in the gene that are associated with an increased risk of developing primary type 3A glaucoma. This information can be used to diagnose the condition early, allowing for prompt treatment and management to prevent vision loss.
NGS testing involves sequencing the entire CYP1B1 gene, which can identify both known and unknown variants. This comprehensive approach can provide more accurate and reliable results compared to traditional genetic testing methods.
It is important to note that while genetic testing can provide valuable information about an individual’s risk of developing primary type 3A glaucoma, it is not a guarantee that the condition will develop. Other factors, such as environmental and lifestyle factors, can also play a role in the development of glaucoma. Therefore, genetic testing should be used in conjunction with regular eye exams and other preventative measures to ensure optimal eye health.
Test Name | CYP1B1 Gene Glaucoma primary type 3A 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 | Ophthalmology Disorders |
Doctor | Ophthalmologist |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for CYP1B1 Gene Glaucoma, primary type 3A NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CYP1B1 Gene Glaucoma, primary type 3A NGS Genetic DNA Test gene CYP1B1 |
Test Details |
The CYP1B1 gene is associated with primary type 3A glaucoma, a rare form of glaucoma that typically affects infants and young children. This condition is characterized by high intraocular pressure, optic nerve damage, and visual impairment. NGS genetic testing for the CYP1B1 gene can identify mutations or variations in the gene that are associated with an increased risk of developing primary type 3A glaucoma. This information can be used to diagnose the condition early, allowing for prompt treatment and management to prevent vision loss. NGS testing involves sequencing the entire CYP1B1 gene, which can identify both known and unknown variants. This comprehensive approach can provide more accurate and reliable results compared to traditional genetic testing methods. It is important to note that while genetic testing can provide valuable information about an individual’s risk of developing primary type 3A glaucoma, it is not a guarantee that the condition will develop. Other factors, such as environmental and lifestyle factors, can also play a role in the development of glaucoma. Therefore, genetic testing should be used in conjunction with regular eye exams and other preventative measures to ensure optimal eye health. |