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Syndrome

Hyper-IgM Immunodeficiency Syndrome

AMW:DIS:150086

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.

Pathology clinical
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Hyper-IgM Immunodeficiency Syndrome has parent Dysgammaglobulinemia
Hyper-IgM Immunodeficiency Syndrome has parent Genetic Diseases, Inborn
Hyper-IgM Immunodeficiency Syndrome, Type 1 has parent Hyper-IgM Immunodeficiency Syndrome
Hyper-IgM Immunodeficiency Syndrome has parent Primary Immunodeficiency Diseases

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