RORC Gene Immunodeficiency type 42 Genetic Test
Test Name: RORC Gene Immunodeficiency type 42 Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
Price: 4400.0 AED
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 RORC Gene Immunodeficiency type 42 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RORC Gene Immunodeficiency type 42 NGS Genetic DNA Test gene RORC
Test Details:
The RORC gene immunodeficiency type 42 NGS genetic test is a type of genetic test that uses next-generation sequencing (NGS) technology to analyze the RORC gene. The RORC gene is responsible for producing a protein called RORt, which plays a crucial role in the development and function of immune cells.
Mutations or variations in the RORC gene can lead to immunodeficiency type 42, which is a rare genetic disorder characterized by a weakened immune system. Individuals with this condition are more susceptible to infections and may have other associated symptoms such as autoimmune diseases or developmental abnormalities.
The NGS genetic test for RORC gene immunodeficiency type 42 involves sequencing the entire coding region of the gene to identify any genetic changes or mutations. This test can help in confirming a diagnosis, providing information on disease prognosis, and guiding treatment decisions.
The test is usually performed on a blood sample or other tissue samples, and the DNA is extracted and sequenced using NGS technology. The resulting sequence data is then compared to a reference sequence to identify any genetic variations or mutations in the RORC gene.
The RORC gene immunodeficiency type 42 NGS genetic test can be ordered by a healthcare provider or genetic counselor if there is a suspicion of this specific genetic disorder based on the patient’s symptoms and medical history. The test results can help in providing a more accurate diagnosis and may also have implications for family planning and genetic counseling.
Test Name | RORC Gene Immunodeficiency type 42 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 RORC Gene Immunodeficiency type 42 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RORC Gene Immunodeficiency type 42 NGS Genetic DNA Test gene RORC |
Test Details |
The RORC gene immunodeficiency type 42 NGS genetic test is a type of genetic test that uses next-generation sequencing (NGS) technology to analyze the RORC gene. The RORC gene is responsible for producing a protein called RORt, which plays a crucial role in the development and function of immune cells. Mutations or variations in the RORC gene can lead to immunodeficiency type 42, which is a rare genetic disorder characterized by a weakened immune system. Individuals with this condition are more susceptible to infections and may have other associated symptoms such as autoimmune diseases or developmental abnormalities. The NGS genetic test for RORC gene immunodeficiency type 42 involves sequencing the entire coding region of the gene to identify any genetic changes or mutations. This test can help in confirming a diagnosis, providing information on disease prognosis, and guiding treatment decisions. The test is usually performed on a blood sample or other tissue samples, and the DNA is extracted and sequenced using NGS technology. The resulting sequence data is then compared to a reference sequence to identify any genetic variations or mutations in the RORC gene. The RORC gene immunodeficiency type 42 NGS genetic test can be ordered by a healthcare provider or genetic counselor if there is a suspicion of this specific genetic disorder based on the patient’s symptoms and medical history. The test results can help in providing a more accurate diagnosis and may also have implications for family planning and genetic counseling. |