IL2RG Gene Combined Immunodeficiency X-Linked Moderate Genetic Test
At DNA Labs UAE, we offer the IL2RG Gene Combined Immunodeficiency X-Linked Moderate Genetic Test to diagnose and identify mutations in the IL2RG gene, which is responsible for this genetic disorder.
Test Details
The IL2RG gene combined immunodeficiency, X-linked, moderate is a genetic disorder that affects the immune system. It is caused by mutations in the IL2RG gene, located on the X chromosome.
Our NGS genetic testing, or next-generation sequencing genetic testing, utilizes advanced sequencing technology to analyze multiple genes simultaneously. In the case of IL2RG gene combined immunodeficiency, X-linked, moderate, this testing involves sequencing the IL2RG gene to identify any mutations or variations present.
Test Components and Price
The IL2RG Gene Combined Immunodeficiency X-Linked Moderate Genetic Test costs AED 4400.0. The test requires a blood sample, extracted DNA, or one drop of blood on an FTA card.
Report Delivery
The test results will be delivered within 3 to 4 weeks after the sample is received.
Test Method
We utilize NGS technology for this genetic test, which allows for comprehensive analysis and accurate identification of mutations in the IL2RG gene.
Test Type and Department
The IL2RG Gene Combined Immunodeficiency X-Linked Moderate Genetic Test falls under the categories of Osteology, Dermatology, and Immunology Disorders. The test is conducted by our Genetics department.
Doctor and Pre-Test Information
A dermatologist will oversee the IL2RG Gene Combined Immunodeficiency X-Linked Moderate Genetic Test. Prior to the test, it is essential 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 IL2RG gene.
Significance of IL2RG Gene Combined Immunodeficiency X-Linked Moderate Genetic Test
This genetic test plays a crucial role in diagnosing IL2RG gene combined immunodeficiency, X-linked, moderate. It helps in identifying mutations in the IL2RG gene and can also determine carrier status in individuals who may pass on the disorder to their children. NGS genetic testing provides valuable information for diagnosis, treatment, and genetic counseling.
| Test Name | IL2RG Gene Combined immunodeficiency X-linked moderate 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 IL2RG Gene Combined immunodeficiency, X-linked, moderate NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with IL2RG Gene Combined immunodeficiency, X-linked, moderate NGS Genetic DNA Test gene IL2RG |
| Test Details |
IL2RG gene combined immunodeficiency, X-linked, moderate is a genetic disorder that affects the immune system. It is caused by mutations in the IL2RG gene, which is located on the X chromosome. NGS genetic testing, or next-generation sequencing genetic testing, is a type of genetic test that uses advanced sequencing technology to analyze multiple genes at once. In the case of IL2RG gene combined immunodeficiency, X-linked, moderate, NGS genetic testing would involve sequencing the IL2RG gene to identify any mutations or variations that may be present. This type of genetic testing can help diagnose IL2RG gene combined immunodeficiency, X-linked, moderate by identifying mutations in the IL2RG gene. It can also be used to determine carrier status in individuals who may be at risk of passing the disorder on to their children. NGS genetic testing is a powerful tool in the field of genetics and can provide valuable information for diagnosis, treatment, and genetic counseling. It allows for the analysis of multiple genes simultaneously, which can be particularly useful in cases where a specific genetic disorder is suspected but the exact gene involved is unknown. |
