Epidermolysis bullosa acquisita
Epidermolysis bullosa acquisita is a chronic subepidermal blistering disease associated with autoimmunity to type VII collagen[2] within anchoring fibril structures that are located at the dermoepidermal junction.[3]:609
| Epidermolysis bullosa acquisita | |
|---|---|
| Other names | Acquired epidermolysis bullosa[1] |
| Specialty | Dermatology  |
See also
References
- RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Acquired epidermolysis bullosa". www.orpha.net. Retrieved 19 April 2019.
- Helen Chapel; Mansel Haeney; Siraj Misbah (2006). Essentials of clinical immunology. Wiley-Blackwell. pp. 207–. ISBN 978-1-4051-2761-5. Retrieved 25 June 2010.
- Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN 978-0-07-138076-8.
External links
| Classification | |
|---|---|
| External resources |
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.