NFKB2 Gene Immunodeficiency Common Variable Type 10 Genetic Test
Are you experiencing recurrent infections and low levels of antibodies in the blood? You may have common variable immunodeficiency type 10 (CVID10), which is associated with the NFKB2 gene. At DNA Labs UAE, we offer a comprehensive NFKB2 Gene Immunodeficiency Common Variable Type 10 Genetic Test to help diagnose and provide appropriate treatment strategies for individuals with CVID10.
Test Details
The NFKB2 gene is associated with a type of immunodeficiency called common variable immunodeficiency type 10 (CVID10). CVID is a group of disorders characterized by recurrent infections and low levels of antibodies in the blood.
NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze the DNA sequence of an individual. It can be used to identify genetic mutations or variations that may be associated with certain diseases or conditions, including immunodeficiencies like CVID10.
NGS genetic testing for the NFKB2 gene can help diagnose individuals with CVID10 by identifying any mutations or variations in the gene that may be causing the immunodeficiency. This information can be useful for determining appropriate treatment strategies and providing genetic counseling to affected individuals and their families.
Test Components and Price
The NFKB2 Gene Immunodeficiency Common Variable Type 10 Genetic Test is priced at 4400.0 AED. The test requires a blood sample, extracted DNA, or one drop of blood on an FTA card.
Report Delivery and Method
Once the sample is collected, the report will be delivered within 3 to 4 weeks. The test is performed using NGS technology, which ensures accurate and reliable results.
Test Type and Referring Doctor
The NFKB2 Gene Immunodeficiency Common Variable Type 10 Genetic Test falls under the category of Osteology Dermatology Immunology Disorders. The test is typically referred by dermatologists due to its association with skin-related symptoms.
Test Department and Pre-Test Information
The NFKB2 Gene Immunodeficiency Common Variable Type 10 Genetic Test is conducted in our Genetics department. Before undergoing the test, it is essential to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by NFKB2 Gene Immunodeficiency Common Variable Type 10 NGS Genetic DNA Test gene NFKB2.
If you suspect that you or a family member may have CVID10, it is crucial to get tested and receive appropriate medical guidance. Contact DNA Labs UAE today to schedule your NFKB2 Gene Immunodeficiency Common Variable Type 10 Genetic Test and take control of your health.
Test Name | NFKB2 Gene Immunodeficiency common variable type 10 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 | Osteology Dermatology Immunology Disorders |
Doctor | Dermatologist |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for NFKB2 Gene Immunodeficiency common variable type 10 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NFKB2 Gene Immunodeficiency common variable type 10 NGS Genetic DNA Test gene NFKB2 |
Test Details |
The NFKB2 gene is associated with a type of immunodeficiency called common variable immunodeficiency type 10 (CVID10). CVID is a group of disorders characterized by recurrent infections and low levels of antibodies in the blood. NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze the DNA sequence of an individual. It can be used to identify genetic mutations or variations that may be associated with certain diseases or conditions, including immunodeficiencies like CVID10. NGS genetic testing for the NFKB2 gene can help diagnose individuals with CVID10 by identifying any mutations or variations in the gene that may be causing the immunodeficiency. This information can be useful for determining appropriate treatment strategies and providing genetic counseling to affected individuals and their families. |