ZNF469 Gene Brittle Cornea Syndrome Genetic Test
Welcome to DNA Labs UAE, where we offer the ZNF469 Gene Brittle Cornea Syndrome Genetic Test. This test is designed to diagnose the rare genetic disorder known as Brittle Cornea Syndrome, which is characterized by thin and fragile corneas that are prone to rupture or tear. By identifying mutations in the ZNF469 gene, we can help individuals and families affected by this condition.
Test Details
The ZNF469 gene is associated with Brittle Cornea Syndrome, a condition that can cause severe vision impairment or even blindness. Our Next-Generation Sequencing (NGS) Genetic Test is a highly accurate and reliable diagnostic tool for identifying mutations in this gene. By sequencing the entire gene, we can detect any variations or mutations that may be responsible for the condition.
NGS Genetic Test is not only useful for diagnosing Brittle Cornea Syndrome, but it can also be used for carrier testing and prenatal diagnosis in families with a history of this condition. Genetic counseling is recommended for individuals and families who undergo NGS Genetic Testing to better understand the implications and potential treatment options.
Test Components and Price
The ZNF469 Gene Brittle Cornea Syndrome Genetic Test is priced at 4400.0 AED. The test requires a blood sample or extracted DNA, or one drop of blood on an FTA card. The report delivery time is typically 3 to 4 weeks, allowing for a comprehensive analysis of the genetic information.
Symptoms and Diagnosis
Brittle Cornea Syndrome is characterized by thin and fragile corneas that can easily rupture or tear. Individuals with this condition may experience severe vision impairment or even blindness. To diagnose Brittle Cornea Syndrome, a clinical history of the patient is taken, and a genetic counseling session is conducted to draw a pedigree chart of family members affected by the condition.
Referring Doctor and Test Department
The ZNF469 Gene Brittle Cornea Syndrome Genetic Test is conducted under the supervision of an ophthalmologist, who specializes in ophthalmology disorders. The test is carried out in our Genetics Test Department, ensuring accurate and reliable results.
Conclusion
The ZNF469 Gene Brittle Cornea Syndrome Genetic Test offered by DNA Labs UAE is a valuable diagnostic tool for individuals and families affected by Brittle Cornea Syndrome. By identifying mutations in the ZNF469 gene, we can provide a comprehensive diagnosis and help determine the best course of treatment. Genetic counseling is recommended for those undergoing NGS Genetic Testing to fully understand the implications of the test results.
| Test Name | ZNF469 Gene Brittle cornea syndrome 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 ZNF469 Gene Brittle cornea syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ZNF469 Gene Brittle cornea syndrome NGS Genetic DNA Test gene ZNF469 |
| Test Details |
The ZNF469 gene is associated with Brittle cornea syndrome, which is a rare genetic disorder characterized by thin and fragile corneas that can easily rupture or tear. This condition can lead to severe vision impairment or even blindness. NGS (Next-Generation Sequencing) Genetic Test is a diagnostic tool that can identify mutations in the ZNF469 gene, which can help in the diagnosis of Brittle cornea syndrome. This test involves sequencing the entire gene to detect any variations or mutations that may be responsible for the condition. NGS Genetic Test is a highly accurate and reliable method for diagnosing genetic disorders, including Brittle cornea syndrome. It can also be used for carrier testing and prenatal diagnosis in families with a history of this condition. Genetic counseling is recommended for individuals and families who undergo NGS Genetic Testing. |
