PAX6 Gene Coloboma ocular autosomal dominant Genetic Test
Are you concerned about the risk of developing coloboma and other ocular anomalies? Genetic testing for the PAX6 gene mutation can provide you with valuable information. At DNA Labs UAE, we offer the PAX6 Gene Coloboma ocular autosomal dominant Genetic Test at a cost of AED 4400.0.
Test Details
The PAX6 gene plays a critical role in the development of the eye and is associated with various eye disorders, including coloboma and ocular anomalies. Coloboma is a congenital defect that leads to incomplete formation of the eye, resulting in a gap or hole in one or more eye structures. Ocular anomalies, on the other hand, encompass a range of eye disorders that affect the structure and function of the eye.
The PAX6 gene mutation is inherited in an autosomal dominant manner, meaning that a single copy of the mutated gene is sufficient to cause the disorder. Our genetic test utilizes Next-generation sequencing (NGS) technology, which allows us to sequence the entire PAX6 gene and accurately detect mutations.
By undergoing this test, individuals with coloboma or other ocular anomalies can receive an early diagnosis and access appropriate medical care and genetic counseling. Additionally, it can help identify family members who may also be at risk for these disorders, enabling them to make informed decisions about family planning.
Test Components and Price
Our PAX6 Gene Coloboma ocular autosomal dominant Genetic Test is priced at AED 4400.0. The test can be conducted using a blood sample, extracted DNA, or even one drop of blood on an FTA Card.
Report Delivery and Method
After undergoing the test, you can expect to receive your report within 3 to 4 weeks. The test is conducted using NGS technology, ensuring accurate and reliable results.
Test Type and Doctor
The PAX6 Gene Coloboma ocular autosomal dominant Genetic Test falls under the category of Ophthalmology Disorders. Our team of experienced ophthalmologists will handle the test and provide you with the necessary guidance and support.
Test Department and Pre-Test Information
The PAX6 Gene Coloboma ocular autosomal dominant Genetic Test is conducted in our Genetics department. Before undergoing the test, it is important to provide a clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by PAX6 Gene Coloboma, ocular, autosomal dominant NGS Genetic DNA Test.
At DNA Labs UAE, we understand the importance of early diagnosis and genetic testing. By offering the PAX6 Gene Coloboma ocular autosomal dominant Genetic Test, we aim to help individuals and families make informed decisions about their eye health and plan for the future.
Test Name | PAX6 Gene Coloboma ocular autosomal dominant 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 PAX6 Gene Coloboma, ocular, autosomal dominant NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PAX6 Gene Coloboma, ocular, autosomal dominant NGS Genetic DNA Test gene PAX6 |
Test Details | The PAX6 gene is a critical gene involved in the development of the eye and is associated with several eye disorders, including coloboma and ocular anomalies. Coloboma is a congenital defect that results in the incomplete formation of the eye, leading to a gap or hole in one or more structures of the eye. Ocular anomalies are a group of eye disorders that affect the structure and function of the eye. The PAX6 gene is inherited in an autosomal dominant manner, which means that a single copy of the mutated gene is sufficient to cause the disorder. Genetic testing for PAX6 gene mutations can help identify individuals who are at risk for developing coloboma and other ocular anomalies. Next-generation sequencing (NGS) is a genetic testing method that can sequence the entire PAX6 gene and detect mutations with high accuracy. This test can help diagnose individuals with coloboma or other ocular anomalies and identify family members who may also be at risk for these disorders. Early diagnosis and genetic testing can help individuals with PAX6 gene mutations receive appropriate medical care and genetic counseling. This can help them better understand their risk for passing on the mutation to their children and make informed decisions about family planning. |