Immunodeficiency with hyperimmunoglobulin M | |
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Other names | Hyper-IgM syndrome type 1[1] |
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This condition is inherited in an X-linked recessive manner | |
Specialty | Medical genetics |
Immunodeficiency with hyperimmunoglobulin M is a rare disorder characterized by recurrent infections, low or absent IgG, IgE, and IgA levels, and normal or elevated levels of IgM and IgD.[2]: 84