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MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 2 ÆäÀÌÁö: 1
  • Hyper-IgM Immunodeficiency Syndrome - »õâ 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.
    Synonyms : HIGM2 Syndrome, HIGM3 Syndrome, HIGM5 Syndrome, Hyper-IgM Immunodeficiency Syndrome Type 2, Hyper-IgM Immunodeficiency Syndrome Type 3, Hyper-IgM Immunodeficiency Syndrome Type 5, Hyper-IgM Syndrome, Hyper-IgM Syndrome 2, Hyper-IgM Syndrome 3, HIGM2 Syndromes
  • Hyper-IgM Immunodeficiency Syndrome, Type 1 - »õâ An X-linked hyper-IgM immunodeficiency subtype resulting from mutation in the gene encoding CD40 LIGAND.
    Synonyms : HIGM1 Syndrome, Hyper-IgM Immunodeficiency, X-Linked, Hyper-IgM Syndrome 1, HIGM1 Syndromes, Hyper IgM Immunodeficiency Syndrome, Type 1, Hyper IgM Immunodeficiency, X Linked, Hyper IgM Syndrome 1, Hyper-IgM Immunodeficiencies, X-Linked, Syndrome 1, Hyper-IgM
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MeSH(Medical Subject Headings) À¯»ç °Ë»ö (http://www.nlm.nih.gov) °á°ú : 0 ÆäÀÌÁö: 1
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