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syndróm imunodeficiencie, hyper-IgM
Č. záznamu d053306 Dátum 06.06.2025 Typ M - MESH Tematický termín syndróm imunodeficiencie, hyper-IgM Iný termín Angličtina (Pseudonym) Hyper-IgM Immunodeficiency Syndrome, Type 2
Angličtina (Pseudonym) Hyper-IgM Immunodeficiency Syndrome, Type 3
Angličtina (Pseudonym) Hyper-IgM Immunodeficiency Syndrome, Type 5
Slovenčina (Pseudonym) syndróm hyper-IgM
Slovenčina (Pseudonym) syndróm imunodeficiencie, hyper-IgM, typ 2
Slovenčina (Pseudonym) syndróm imunodeficiencie, hyper-IgM, typ 3
Slovenčina (Pseudonym) syndróm imunodeficiencie, hyper-IgM, typ 5
MDT C15.378.147.333.249C16.320.413C16.320.798.625C20.673.430.250C20.673.795.625 Poznámka A 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. predmetové heslo
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