Short Description

NGS genetic DNA test detecets for variant and mutation detection in CD96 gene for C syndrome

PreTest Information

Clinical History of Patient who is going for CD96 Gene C syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CD96 Gene C syndrome NGS Genetic DNA Test gene CD96

Detail Description

Understanding CD96 Gene C Syndrome: Symptoms, Diagnosis, and DNA Testing Cost

CD96 Gene C Syndrome, also known as T-cell immunoreceptor with Ig and ITIM domains (TIGIT) deficiency, is a rare genetic disorder that affects the immune system. It is caused by mutations in the CD96 gene, which provides instructions for making a protein that plays a critical role in regulating the activity of immune cells.

Individuals with CD96 Gene C Syndrome have a weakened immune system, making them more susceptible to infections. They may also experience autoimmune disorders, where the immune system attacks healthy cells in the body.

Symptoms of CD96 Gene C Syndrome

The symptoms of CD96 Gene C Syndrome can vary from person to person. Some individuals may have mild symptoms, while others may experience severe complications. Common symptoms of CD96 Gene C Syndrome include:

• Recurrent infections, such as respiratory infections and ear infections
• Autoimmune disorders, such as inflammatory bowel disease, lupus, or rheumatoid arthritis
• Delayed growth and development
• Frequent or severe skin infections
• Abnormalities in the immune system, such as low levels of certain immune cells

Diagnosis of CD96 Gene C Syndrome

Diagnosing CD96 Gene C Syndrome can be challenging, as it is a rare disorder. However, a variety of tests can be used to diagnose the condition, including:

• Genetic testing: A blood sample is taken and analyzed for mutations in the CD96 gene.
• Immunological testing: Blood tests can measure the levels of different immune cells and antibodies to determine if there are any abnormalities in the immune system.
• Medical history and physical exam: A doctor may ask about the individual's medical history and perform a physical exam to look for signs of infections or autoimmune disorders.

DNA Testing Cost for CD96 Gene C Syndrome

The cost of DNA testing for CD96 Gene C Syndrome can vary depending on the type of test and where it is performed. In India, the cost of Next Generation Sequencing (NGS) genetic testing for CD96 Gene C Syndrome is typically around INR 20,000.

Conclusion

CD96 Gene C Syndrome is a rare genetic disorder that affects the immune system. Individuals with CD96 Gene C Syndrome may experience recurrent infections, autoimmune disorders, and delayed growth and development. Diagnosing the condition can be challenging, but genetic testing and immunological testing can be used to identify mutations in the CD96 gene and abnormalities in the immune system. The cost of DNA testing for CD96 Gene C Syndrome in India is typically around INR 20,000.

If you suspect that you or a loved one may have CD96 Gene C Syndrome, it is important to speak with a healthcare provider. DNA Labs India offers NGS genetic testing for CD96 Gene C Syndrome, as well as a range of other genetic disorders. Contact us today to learn more.

The CD96 gene encodes a protein known as T-cell-activated increased late expression (TACTILE), which is involved in immune cell interactions and communication.

NGS (Next-Generation Sequencing) genetic DNA tests are used to analyze the DNA sequence of genes like CD96 to identify any mutations or variants that may be associated with C syndrome.

If you or someone you know is considering genetic testing for C syndrome related to the CD96 gene, I recommend consulting with a medical geneticist, a pediatrician, or a genetic counselor. They can provide accurate and current information about the condition, the implications of genetic testing, and any available treatment options. Medical knowledge can evolve, so it's important to rely on expert guidance for the latest information.