مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Information Journal Paper

Title

The Genetic Heterogeneity of Common Variable Immunodeficiency (CVID)

Pages

  8-16

Abstract

 CVID represents the most frequent symptomatic primary humoral immunodeficiency. Clinical presentation includes hypogammaglobulinemia, recurrent infections, autoimmune phaenomena and increased lymphoma and cancer risk. While the first cases were reported in the early 50’ s, the first genetic cause of CVID was described after 5 decades. After the first description, and also thanks to the advances in the field of biomedical research, several additional genetic causes of CVID have been described. The current genetic landscape of CVID includes numerous genetic alterations that may cause or contribute to the development of CVID, underscoring the complexity and heterogeneity of this disorder.

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    • References

    Cite

    APA: Copy

    Lougaris, Vasssilios, & Plebani, Alessandro. (2020). The Genetic Heterogeneity of Common Variable Immunodeficiency (CVID). IMMUNOLOGY AND GENETICS JOURNA, 3(1), 8-16. SID. https://sid.ir/paper/754219/en

    Vancouver: Copy

    Lougaris Vasssilios, Plebani Alessandro. The Genetic Heterogeneity of Common Variable Immunodeficiency (CVID). IMMUNOLOGY AND GENETICS JOURNA[Internet]. 2020;3(1):8-16. Available from: https://sid.ir/paper/754219/en

    IEEE: Copy

    Vasssilios Lougaris, and Alessandro Plebani, “The Genetic Heterogeneity of Common Variable Immunodeficiency (CVID),” IMMUNOLOGY AND GENETICS JOURNA, vol. 3, no. 1, pp. 8–16, 2020, [Online]. Available: https://sid.ir/paper/754219/en

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