Immunodeficiency with hyperimmunoglobulin M information
Rare disorder
Medical condition
Immunodeficiency with hyperimmunoglobulin M
Other names
Hyper-IgM syndrome type 1[1]
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
^"X-linked hyper-IgM syndrome". Orphanet. Retrieved 18 March 2019.
^James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 978-0-7216-2921-6.
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