RFX5 Gene Bare Lymphocyte Syndrome Type 2 Complementation Group C Genetic Test
At DNA Labs UAE, we offer the RFX5 Gene Bare Lymphocyte Syndrome Type 2 Complementation Group C Genetic Test. This test is designed to analyze the DNA sequence of the RFX5 gene and identify any mutations or variations that may be responsible for Bare Lymphocyte Syndrome Type 2 Complementation Group C.
Test Details
The RFX5 gene is associated with Bare Lymphocyte Syndrome Type 2 Complementation Group C, a genetic disorder that affects the immune system. It impairs the ability of lymphocytes, a type of white blood cell, to respond to infections. Our Next-Generation Sequencing (NGS) technology allows us to analyze the individual’s DNA and provide information about specific genetic changes in the RFX5 gene.
Symptoms and Diagnosis
Bare Lymphocyte Syndrome Type 2 Complementation Group C can cause various symptoms, including recurrent infections, impaired immune response, and susceptibility to opportunistic infections. To diagnose this condition, a clinical history of the patient is taken into account. A genetic counseling session may also be conducted to draw a pedigree chart of family members affected by this syndrome.
Test Components and Price
The RFX5 Gene Bare Lymphocyte Syndrome Type 2 Complementation Group C Genetic Test costs 4400.0 AED. The sample condition required for this test can be either blood, extracted DNA, or one drop of blood on an FTA card.
Report Delivery and Method
After the sample is collected, the report will be delivered within 3 to 4 weeks. The test is performed using NGS technology, which allows for accurate and comprehensive analysis of the RFX5 gene.
Test Type and Doctor
The RFX5 Gene Bare Lymphocyte Syndrome Type 2 Complementation Group C Genetic Test falls under the category of Hematology tests. It is recommended to consult a hematologist for this specific test.
Test Department and Pre-Test Information
This genetic test is conducted in our Genetics department. It is important to provide the clinical history of the patient who is undergoing the test, especially if they have a family history of Bare Lymphocyte Syndrome Type 2 Complementation Group C. Genetic counseling may also be beneficial to understand the implications of the test results.
Conclusion
The RFX5 Gene Bare Lymphocyte Syndrome Type 2 Complementation Group C Genetic Test offered by DNA Labs UAE is a valuable tool for diagnosing and understanding this genetic disorder. It can provide important information about specific genetic changes in the RFX5 gene, which can aid in confirming a diagnosis and making informed decisions regarding carrier testing, family planning, and genetic counseling.
| Test Name | RFX5 Gene Bare lymphocyte syndrome type 2 complementation group C 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 | Hematology |
| Doctor | Hematologist |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for RFX5 Gene Bare lymphocyte syndrome, type 2, complementation group C NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RFX5 Gene Bare lymphocyte syndrome, type 2, complementation group C NGS Genetic DNA Test gene RFX5 |
| Test Details | The RFX5 gene is associated with a condition called Bare lymphocyte syndrome, type 2, complementation group C. This genetic disorder affects the immune system and impairs the ability of lymphocytes (a type of white blood cell) to respond to infections. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of a person’s genes. In the context of Bare lymphocyte syndrome, NGS genetic testing can be used to identify mutations or variations in the RFX5 gene that may be responsible for the condition. By analyzing the individual’s DNA, NGS can provide information about specific genetic changes in the RFX5 gene, which can help in confirming a diagnosis of Bare lymphocyte syndrome, type 2, complementation group C. This testing can also be useful for carrier testing, family planning, and genetic counseling. It’s important to note that NGS genetic testing is typically performed by a medical professional or genetic counselor, and the results should be interpreted in consultation with a healthcare provider who specializes in genetics. |
