Sale!

TNFRSF13C Gene Immunodeficiency common variable type 4 Genetic Test Cost

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

-21%

The TNFRSF13C gene plays a crucial role in the immune system, specifically in the functioning of B cells, which are essential for producing antibodies. Mutations in this gene can lead to Immunodeficiency Common Variable Type 4 (CVID4), a type of primary immunodeficiency disorder. This condition is characterized by a marked decrease in the level of immunoglobulins (antibodies) in the blood, leading to an increased susceptibility to infections.

The genetic test for TNFRSF13C gene mutations is a critical tool in diagnosing CVID4. It involves analyzing the DNA to identify any abnormalities in the TNFRSF13C gene that could be responsible for the disorder. This test is crucial for confirming the diagnosis, which can significantly impact the management and treatment plans for affected individuals.

At DNA Labs UAE, the TNFRSF13C Gene Immunodeficiency Common Variable Type 4 Genetic Test is available for individuals who are suspected of having this condition or for those with a family history of immunodeficiency disorders. The test is priced at 4400 AED. Conducting this test in a specialized facility like DNA Labs UAE ensures accuracy and reliability of results, which are critical for making informed medical decisions.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

TNFRSF13C Gene Immunodeficiency common variable type 4 Genetic Test

At DNA Labs UAE, we offer the TNFRSF13C Gene Immunodeficiency common variable type 4 Genetic Test. This test is used to diagnose a type of primary immunodeficiency disorder caused by mutations in the TNFRSF13C gene.

Test Components and Price

  • Components: TNFRSF13C Gene Immunodeficiency common variable type 4 Genetic Test
  • Price: 4400.0 AED

Sample Condition and Report Delivery

  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks

Method and Test Type

  • Method: NGS Technology (Next-Generation Sequencing)
  • Test Type: Osteology Dermatology Immunology Disorders

Doctor and Test Department

  • Doctor: Dermatologist
  • Test Department: Genetics

Pre Test Information

Before undergoing the TNFRSF13C Gene Immunodeficiency common variable type 4 Genetic Test, it is important to provide the clinical history of the patient. A Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with TNFRSF13C Gene Immunodeficiency common variable type 4 NGS Genetic DNA Test gene TNFRSF13C.

Test Details

TNFRSF13C gene immunodeficiency common variable type 4 is a type of primary immunodeficiency disorder caused by mutations in the TNFRSF13C gene. This gene is responsible for producing a protein called BAFF receptor, which plays a role in the development and survival of certain immune cells.

NGS genetic testing, using advanced sequencing technology, can analyze multiple genes simultaneously. In the case of TNFRSF13C gene immunodeficiency common variable type 4, NGS genetic testing can identify mutations in the TNFRSF13C gene that may be responsible for the disorder.

NGS genetic testing is useful for diagnosing TNFRSF13C gene immunodeficiency common variable type 4 by detecting mutations in the TNFRSF13C gene. It can also be used for carrier testing in individuals with a family history of the disorder and for prenatal testing in families with a known mutation.

The results of NGS genetic testing provide important information for the management and treatment of individuals with TNFRSF13C gene immunodeficiency common variable type 4. It helps in determining appropriate treatment strategies and identifying other family members who may be at risk for the disorder.

Test Name TNFRSF13C Gene Immunodeficiency common variable type 4 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 TNFRSF13C Gene Immunodeficiency common variable type 4 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TNFRSF13C Gene Immunodeficiency common variable type 4 NGS Genetic DNA Test gene TNFRSF13C
Test Details

TNFRSF13C gene immunodeficiency common variable type 4 is a type of primary immunodeficiency disorder caused by mutations in the TNFRSF13C gene. This gene provides instructions for producing a protein called BAFF receptor, which is involved in the development and survival of certain immune cells.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of TNFRSF13C gene immunodeficiency common variable type 4, NGS genetic testing can be used to identify mutations in the TNFRSF13C gene that may be responsible for the disorder.

NGS genetic testing can help in the diagnosis of TNFRSF13C gene immunodeficiency common variable type 4 by detecting mutations in the TNFRSF13C gene that may be causing the disorder. It can also be used for carrier testing in individuals with a family history of the disorder, as well as for prenatal testing in families with a known mutation.

The results of NGS genetic testing can provide important information for the management and treatment of individuals with TNFRSF13C gene immunodeficiency common variable type 4. It can help in determining the appropriate treatment strategies and in identifying other family members who may be at risk for the disorder.