Immunodeficiency with hyperimmunoglobulin M

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

Immunodeficiency with hyperimmunoglobulin M
Other namesHyper-IgM syndrome type 1[1]
This condition is inherited in an X-linked recessive manner

See also

References
  1. "X-linked hyper-IgM syndrome". Orphanet. Retrieved 18 March 2019.
  2. James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 978-0-7216-2921-6.







Classification
External resources


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