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syndróm imunodeficiencie, hyper-IgM

  1. Record numberd053306
    Date06.06.2025
    TypeM - MESH
    Topical termsyndróm imunodeficiencie, hyper-IgM
    Other termEnglish (Pseudonym) Hyper-IgM Immunodeficiency Syndrome, Type 2
    English (Pseudonym) Hyper-IgM Immunodeficiency Syndrome, Type 3
    English (Pseudonym) Hyper-IgM Immunodeficiency Syndrome, Type 5
    Slovak (Pseudonym) syndróm hyper-IgM
    Slovak (Pseudonym) syndróm imunodeficiencie, hyper-IgM, typ 2
    Slovak (Pseudonym) syndróm imunodeficiencie, hyper-IgM, typ 3
    Slovak (Pseudonym) syndróm imunodeficiencie, hyper-IgM, typ 5
    UDCC15.378.147.333.249C16.320.413C16.320.798.625C20.673.430.250C20.673.795.625
    NoteA rare inherited immunodeficiency syndrome characterized by normal or elevated serum IMMUNOGLOBULIN M levels with absence of IMMUNOGLOBULIN G; IMMUNOGLOBULIN A; and IMMUNOGLOBULIN E. It results in a profound susceptibility to BACTERIAL INFECTIONS and an increased susceptibility to OPPORTUNISTIC INFECTIONS. Several subtypes of hyper-IgM immunodeficiency syndrome exist depending upon the location of genetic mutation.
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Number of the records: 1  

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