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RFX5 Gene Bare Lymphocyte Syndrome Type 2 Complementation Group C Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The “RFX5 Gene Bare Lymphocyte Syndrome Type 2 Complementation Group C Genetic Test” is a specialized diagnostic examination conducted at DNA Labs UAE. This test is designed to identify mutations in the RFX5 gene, which are associated with Bare Lymphocyte Syndrome Type 2, Complementation Group C. Bare Lymphocyte Syndrome Type 2 is a rare immunodeficiency disorder characterized by a reduced expression of Major Histocompatibility Complex (MHC) class II molecules, leading to a severe impairment in the immune system’s ability to fight infections. The RFX5 gene plays a crucial role in the regulation of MHC class II genes, and mutations in this gene can disrupt this process, leading to the condition.

The test involves collecting a DNA sample, typically through a blood draw, and analyzing it for specific genetic alterations in the RFX5 gene that are known to cause the syndrome. It is a critical tool for the diagnosis and management of individuals suspected to have this condition, enabling healthcare providers to tailor treatment strategies according to the genetic makeup of the patient.

The cost of the test is set at 4400 AED, reflecting the specialized nature of the genetic analysis and the expertise required to interpret the results accurately. Conducted at DNA Labs UAE, a facility renowned for its advanced genetic testing capabilities and commitment to providing high-quality healthcare services, this test represents a crucial step forward in the personalized treatment of immune disorders.

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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.

SKU: TEST-3870 Category:

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