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ZNF469 Gene Brittle Cornea Syndrome Genetic Test Cost

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

-21%

The ZNF469 gene plays a crucial role in the structural integrity of the cornea, and mutations in this gene can lead to Brittle Cornea Syndrome (BCS), a rare genetic disorder characterized by thinning and increased fragility of the cornea that can lead to severe visual impairment. The ZNF469 Gene Brittle Cornea Syndrome Genetic Test is a specialized diagnostic tool designed to detect mutations in the ZNF469 gene, aiding in the diagnosis of BCS. This test is crucial for individuals with a family history of BCS or those exhibiting symptoms, as early diagnosis can lead to interventions that may preserve vision and prevent complications.

The test is available at DNA Labs UAE, a leading genetic testing facility known for its state-of-the-art technology and expertise in genetic diagnostics. The cost of the ZNF469 Gene Brittle Cornea Syndrome Genetic Test is 4400 AED. This investment covers the comprehensive analysis required to accurately identify the presence of ZNF469 gene mutations. Given the complexity and rarity of the condition, having access to such a targeted genetic test is invaluable for affected individuals and their families, offering them a clear path towards understanding their condition and exploring potential management strategies.

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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.