DCLRE1C Gene Omenn Syndrome Genetic Test
Welcome to DNA Labs UAE’s blog on the DCLRE1C gene and Omenn syndrome genetic test. In this article, we will discuss the components, cost, symptoms, diagnosis, and other important details related to this test.
Test Details
The DCLRE1C gene is associated with a rare genetic disorder called Omenn syndrome. This autosomal recessive disorder affects the immune system and leads to severe combined immunodeficiency (SCID). To diagnose Omenn syndrome, DNA Labs UAE offers a genetic test using Next-Generation Sequencing (NGS) technology.
Components
- Test Name: DCLRE1C Gene Omenn syndrome Genetic Test
- 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
Prior to the DCLRE1C Gene Omenn syndrome Genetic Test, it is essential to provide the clinical history of the patient. Additionally, a genetic counseling session is recommended to draw a pedigree chart of family members affected by the DCLRE1C gene and Omenn syndrome. This information will aid in the interpretation of the test results.
Test Procedure
The genetic test for Omenn syndrome using NGS involves obtaining a DNA sample, typically through a blood or saliva sample. The DCLRE1C gene is then sequenced using NGS technology. The results of the test can be analyzed to identify any mutations or variants in the gene that may be associated with Omenn syndrome.
Uses of the Test
The DCLRE1C Gene Omenn syndrome Genetic Test can be helpful in diagnosing Omenn syndrome in individuals with symptoms suggestive of the disorder. It can also be used for carrier testing in individuals with a family history of Omenn syndrome. Additionally, prenatal testing can be performed using NGS to determine if a fetus has inherited mutations in the DCLRE1C gene.
It is important to note that genetic testing for Omenn syndrome using NGS should always be done under the guidance of a healthcare professional or genetic counselor. They can help interpret the results and provide appropriate counseling and management options.
Thank you for reading our blog on the DCLRE1C Gene Omenn syndrome Genetic Test. If you have any further questions or would like to schedule a test, please contact DNA Labs UAE.
| Test Name | DCLRE1C Gene Omenn 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 | Osteology Dermatology Immunology Disorders |
| Doctor | Dermatologist |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for DCLRE1C Gene Omenn syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with DCLRE1C Gene Omenn syndrome NGS Genetic DNA Test gene DCLRE1C |
| Test Details |
The DCLRE1C gene is associated with a rare genetic disorder called Omenn syndrome. Omenn syndrome is an autosomal recessive disorder that affects the immune system, leading to severe combined immunodeficiency (SCID). NGS (Next-Generation Sequencing) is a genetic testing technique that allows for the simultaneous analysis of multiple genes or the entire genome. In the context of Omenn syndrome, NGS can be used to identify mutations or variants in the DCLRE1C gene that may be responsible for the disorder. Genetic testing for Omenn syndrome using NGS involves obtaining a DNA sample, typically through a blood or saliva sample, and sequencing the DCLRE1C gene using NGS technology. The results of the test can then be analyzed to identify any mutations or variants in the gene that may be associated with Omenn syndrome. This genetic test can be helpful in diagnosing Omenn syndrome in individuals with symptoms suggestive of the disorder and can also be used for carrier testing in individuals with a family history of Omenn syndrome. Additionally, prenatal testing can be performed using NGS to determine if a fetus has inherited mutations in the DCLRE1C gene. It is important to note that genetic testing for Omenn syndrome using NGS should be done under the guidance of a healthcare professional or genetic counselor who can help interpret the results and provide appropriate counseling and management options. |
