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 names | Hyper-IgM syndrome type 1[1] |
 | |
| This condition is inherited in an X-linked recessive manner | |
References
- "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.
External links
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.