Epidermolysis bullosa acquisita
From Wikipedia, the free encyclopedia
| Epidermolysis bullosa acquisita | |
|---|---|
| Classification and external resources | |
| ICD-10 | L12.3 |
| ICD-9 | 694.8 |
| DiseasesDB | 4338 |
| eMedicine | article/1063083 |
| MeSH | D016107 |
Epidermolysis bullosa acquisita is a chronic subepidermal blistering disease associated with autoimmunity to type VII collagen[1] within anchoring fibril structures that are located at the dermoepidermal junction.[2]:609
See also
- Epidermolysis bullosa
- List of cutaneous conditions
- List of target antigens in pemphigoid
- List of immunofluorescence findings for autoimmune bullous conditions
- List of human leukocyte antigen alleles associated with cutaneous conditions
References
- ↑ 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.
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