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NOD2 Gene Blau Syndrome Genetic Test Cost

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

-21%

The NOD2 Gene Blau Syndrome Genetic Test is a specialized diagnostic assessment offered by DNA Labs UAE, designed to identify mutations in the NOD2 gene, which are linked to Blau syndrome. Blau syndrome is a rare genetic condition characterized by a triad of symptoms: granulomatous arthritis, uveitis, and dermatitis. This autosomal dominant disorder necessitates early and accurate diagnosis to manage symptoms and prevent severe complications effectively.

DNA Labs UAE, leveraging advanced genetic testing technologies, provides this test at a cost of 4400 AED. The test involves collecting a DNA sample from the patient, typically through a blood draw or cheek swab, which is then analyzed in the laboratory to detect the presence of specific mutations in the NOD2 gene that are associated with Blau syndrome. This precise genetic testing allows for a definitive diagnosis, enabling tailored treatment plans and genetic counseling for affected individuals and their families.

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NOD2 Gene Blau Syndrome Genetic Test

At DNA Labs UAE, we offer the NOD2 Gene Blau Syndrome Genetic Test. This test analyzes the NOD2 gene for mutations associated with Blau syndrome. Blau syndrome is a rare genetic disorder characterized by inflammation in various organs, including the skin, joints, and eyes.

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

Prior to undergoing the NOD2 Gene Blau Syndrome Genetic Test, it is important to provide the clinical history of the patient who will be tested. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with NOD2 Gene Blau Syndrome.

Test Details

The NOD2 Gene Blau Syndrome Genetic Test utilizes Next-Generation Sequencing (NGS) technology. NGS is a high-throughput DNA sequencing technology that allows for the rapid and cost-effective analysis of large amounts of genetic information.

The NOD2 gene provides instructions for making a protein involved in the immune system’s response to bacterial infections. Mutations in this gene can disrupt the normal functioning of the protein, leading to an overactive immune response and the development of Blau syndrome.

The NOD2 Gene Blau Syndrome NGS Genetic Test involves sequencing the NOD2 gene to identify any disease-causing mutations. This test can help confirm a diagnosis of Blau syndrome in individuals with symptoms consistent with the condition. It can also be used for carrier testing in individuals with a family history of Blau syndrome to determine if they have a mutation in the NOD2 gene.

Overall, the NOD2 Gene Blau Syndrome NGS Genetic Test plays a crucial role in the diagnosis and management of Blau syndrome. Early detection through this test allows for appropriate treatment strategies to be implemented.

Test Name NOD2 Gene Blau 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 NOD2 Gene Blau syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NOD2 Gene Blau syndrome NGS Genetic DNA Test gene NOD2
Test Details

NOD2 gene Blau syndrome NGS genetic test is a genetic test that analyzes the NOD2 gene for mutations associated with Blau syndrome. Blau syndrome is a rare genetic disorder characterized by inflammation in various organs, including the skin, joints, and eyes.

The NOD2 gene provides instructions for making a protein involved in the immune system’s response to bacterial infections. Mutations in this gene can disrupt the normal functioning of the protein, leading to an overactive immune response and the development of Blau syndrome.

NGS (Next-Generation Sequencing) is a high-throughput DNA sequencing technology that allows for the rapid and cost-effective analysis of large amounts of genetic information. In the case of the NOD2 gene Blau syndrome NGS genetic test, it involves sequencing the NOD2 gene to identify any disease-causing mutations.

This genetic test can help confirm a diagnosis of Blau syndrome in individuals with symptoms consistent with the condition. It can also be used for carrier testing in individuals with a family history of Blau syndrome to determine if they have a mutation in the NOD2 gene.

Overall, the NOD2 gene Blau syndrome NGS genetic test plays a crucial role in the diagnosis and management of Blau syndrome, allowing for early detection and appropriate treatment strategies.

SKU: TEST-4009 Category:

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