Immunodeficiency with hyperimmunoglobulin M
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| 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
See also
[edit]References
[edit]- ^ "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.