PAX2 Gene Papillorenal Syndrome Genetic Test
Welcome to DNA Labs UAE, where we offer advanced genetic testing services. One of the tests we provide is the PAX2 Gene Papillorenal Syndrome Genetic Test. This test helps in diagnosing and determining the specific genetic cause of papillorenal syndrome, a genetic disorder that affects the development of the kidneys and eyes.
Test Details
The PAX2 gene is responsible for producing a protein called paired box protein 2. This protein plays a crucial role in the development of the kidneys, eyes, and ears. Mutations in the PAX2 gene can lead to papillorenal syndrome, also known as renal-coloboma syndrome.
Our PAX2 Gene Papillorenal Syndrome Genetic Test utilizes NGS (Next-Generation Sequencing) technology, which allows for the simultaneous analysis of multiple genes. This advanced sequencing method helps identify any mutations or changes in the DNA sequence of the PAX2 gene.
Test Components and Price
The cost of the PAX2 Gene Papillorenal Syndrome Genetic Test is AED 4400.0. The test can be performed using a blood sample, extracted DNA, or a single drop of blood on an FTA card.
Report Delivery and Method
After the test is conducted, the report will be delivered within 3 to 4 weeks. The NGS technology ensures accurate and comprehensive analysis of the PAX2 gene.
Test Type and Doctor
The PAX2 Gene Papillorenal Syndrome Genetic Test falls under the category of dysmorphology. Our team of experienced pediatric doctors specializes in conducting this test.
Test Department and Pre-Test Information
The PAX2 Gene Papillorenal Syndrome Genetic Test is conducted in our Genetics department. Before undergoing the 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 the disorder.
Conclusion
The PAX2 Gene Papillorenal Syndrome Genetic Test offered by DNA Labs UAE is a reliable and accurate method for diagnosing papillorenal syndrome. By analyzing the PAX2 gene using NGS technology, we can identify any mutations or changes in its DNA sequence, providing valuable insights into the specific genetic cause of the disorder. If you suspect that you or a family member may have papillorenal syndrome, we encourage you to consider our genetic testing services.
Test Name | PAX2 Gene Papillorenal 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 | Dysmorphology |
Doctor | Pediatrics |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for PAX2 Gene Papillorenal syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PAX2 Gene Papillorenal syndrome NGS Genetic DNA Test gene PAX2 |
Test Details |
The PAX2 gene is a gene that provides instructions for making a protein called paired box protein 2. This protein is involved in the development of the kidneys, eyes, and ears. Papillorenal syndrome, also known as renal-coloboma syndrome, is a genetic disorder that affects the development of the kidneys and eyes. It is caused by mutations in the PAX2 gene. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. It allows for the detection of mutations or changes in the DNA sequence of specific genes, including the PAX2 gene. Therefore, a PAX2 gene NGS genetic test would involve sequencing the PAX2 gene to identify any mutations or changes in its DNA sequence. This test can help in diagnosing papillorenal syndrome and determining the specific genetic cause of the disorder. |