Short Description

NGS genetic DNA test detecets for variant and mutation detection in RAG2 gene for Omenn syndrome

PreTest Information

Clinical History of Patient who is going for RAG2 Gene Omenn syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RAG2 Gene Omenn syndrome NGS Genetic DNA Test gene RAG2

Detail Description

Understanding RAG2 Gene and Omenn Syndrome: Symptoms, Diagnosis and NGS Genetic DNA Test Cost

Omenn Syndrome is a rare and severe form of combined immunodeficiency. It is caused by mutations in the RAG2 gene, which plays a crucial role in the development and function of the immune system. In this blog, we will discuss the symptoms and diagnosis of Omenn Syndrome, as well as the NGS Genetic DNA Test cost in India.

Symptoms of Omenn Syndrome

Omenn Syndrome is characterized by a combination of symptoms that affect multiple systems of the body. Some of the common symptoms include:

• Severe eczema and skin rashes
• Enlarged lymph nodes and spleen
• Chronic diarrhea
• Failure to thrive
• Recurrent infections

These symptoms can appear in the first few months of life and can be life-threatening if left untreated. Omenn Syndrome is a medical emergency and requires immediate attention.

Diagnosis of Omenn Syndrome

The diagnosis of Omenn Syndrome involves a combination of clinical evaluation, laboratory tests, and genetic testing. The clinical evaluation includes a physical examination and a review of the patient's medical history. Laboratory tests may include blood tests, immunological tests, and imaging studies.

The genetic testing is essential for confirming the diagnosis of Omenn Syndrome. It involves analyzing the RAG2 gene for mutations using Next-Generation Sequencing (NGS) technology. NGS is a powerful tool that can sequence the entire genome in a short amount of time, making it an efficient and cost-effective method for genetic testing.

NGS Genetic DNA Test Cost in India

The cost of NGS Genetic DNA Test for Omenn Syndrome in India is approximately INR 20,000. This cost may vary depending on the laboratory and the specific tests ordered. However, it is important to note that the cost of genetic testing should not be a barrier to obtaining a proper diagnosis and treatment for Omenn Syndrome.

Genetic testing is a critical component of the diagnosis and treatment of Omenn Syndrome. It can help identify the underlying genetic mutations and guide appropriate treatment decisions. If you suspect that you or your child may have Omenn Syndrome, it is essential to seek medical attention and undergo genetic testing as soon as possible.

Conclusion

Omenn Syndrome is a rare and severe form of combined immunodeficiency that is caused by mutations in the RAG2 gene. The symptoms of Omenn Syndrome can be life-threatening if left untreated, and early diagnosis is essential for proper treatment. Next-Generation Sequencing (NGS) technology is a powerful tool for genetic testing, and the cost of NGS Genetic DNA Test for Omenn Syndrome in India is approximately INR 20,000. If you suspect that you or your child may have Omenn Syndrome, it is crucial to seek medical attention and undergo genetic testing as soon as possible.

At DNA Labs India, we offer a comprehensive range of genetic testing services, including Next-Generation Sequencing (NGS) technology for the diagnosis of genetic disorders. Our team of experienced genetic counselors and scientists are dedicated to providing accurate and timely results to our patients. Contact us today to learn more about our genetic testing services.