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CD40 Gene Immunodeficiency Type 3 with Hyper-IgM Genetic Test Cost

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

-21%

The “CD40 Gene Immunodeficiency Type 3 with Hyper-IgM Genetic Test” is a specialized diagnostic procedure designed to identify mutations in the CD40 gene, which are implicated in a rare form of immunodeficiency known as Hyper-IgM Syndrome Type 3. This condition is characterized by a defective immune response, primarily affecting the body’s ability to produce antibodies against pathogens. Patients typically present with recurrent infections, due to their inability to switch from the production of immunoglobulin M (IgM) to other types of immunoglobulins (e.g., IgG, IgA, IgE) that are essential for a comprehensive immune defense.

Conducted at DNA Labs UAE, this genetic test is a critical tool for the early detection and management of the condition, allowing for tailored treatment plans that can significantly improve the quality of life for affected individuals. The test involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed for specific mutations in the CD40 gene that are known to cause the syndrome.

The cost of the test is set at 4400 AED, reflecting the specialized nature of the analysis and the sophisticated technology employed in detecting the genetic abnormalities associated with this immunodeficiency. Early diagnosis through this test can be pivotal in initiating appropriate interventions, including immunoglobulin replacement therapy and other supportive measures, to mitigate the impact of the disease.

Description

CD40 Gene Immunodeficiency type 3 with hyper-IgM Genetic Test

Test Name: CD40 Gene Immunodeficiency type 3 with hyper-IgM Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

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 CD40 Gene Immunodeficiency type 3, with hyper-IgM NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CD40 Gene Immunodeficiency type 3, with hyper-IgM NGS Genetic DNA Test gene CD40

Test Details: CD40 gene immunodeficiency type 3, with hyper-IgM is a rare genetic disorder that affects the immune system. It is caused by mutations in the CD40 gene, which plays a crucial role in the activation of immune cells. People with CD40 gene immunodeficiency type 3 have a deficiency in the CD40 protein, leading to impaired immune responses. This results in an increased susceptibility to infections, particularly bacterial infections, as well as other immune-related disorders.

The diagnosis of CD40 gene immunodeficiency type 3, with hyper-IgM, can be confirmed through genetic testing. Next-generation sequencing (NGS) is a type of genetic test that allows for the simultaneous analysis of multiple genes, including the CD40 gene. NGS can identify mutations or variations in the CD40 gene that are associated with this immunodeficiency disorder.

Genetic testing for CD40 gene immunodeficiency type 3, with hyper-IgM, can help in the early diagnosis and management of the condition. It can also provide information for genetic counseling and family planning. It is important to note that genetic testing should be conducted by a qualified healthcare professional or genetic counselor who can interpret the results accurately and provide appropriate recommendations based on the findings.

Test Name	CD40 Gene Immunodeficiency type 3 with hyper-IgM 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 CD40 Gene Immunodeficiency type 3, with hyper-IgM NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CD40 Gene Immunodeficiency type 3, with hyper-IgM NGS Genetic DNA Test gene CD40
Test Details	CD40 gene immunodeficiency type 3, with hyper-IgM is a rare genetic disorder that affects the immune system. It is caused by mutations in the CD40 gene, which plays a crucial role in the activation of immune cells. People with CD40 gene immunodeficiency type 3 have a deficiency in the CD40 protein, leading to impaired immune responses. This results in an increased susceptibility to infections, particularly bacterial infections, as well as other immune-related disorders. The diagnosis of CD40 gene immunodeficiency type 3, with hyper-IgM, can be confirmed through genetic testing. Next-generation sequencing (NGS) is a type of genetic test that allows for the simultaneous analysis of multiple genes, including the CD40 gene. NGS can identify mutations or variations in the CD40 gene that are associated with this immunodeficiency disorder. Genetic testing for CD40 gene immunodeficiency type 3, with hyper-IgM, can help in the early diagnosis and management of the condition. It can also provide information for genetic counseling and family planning. It is important to note that genetic testing should be conducted by a qualified healthcare professional or genetic counselor who can interpret the results accurately and provide appropriate recommendations based on the findings.