Epidermolysis bullosa acquisita
| Epidermolysis bullosa acquisita | |
|---|---|
| Other names | Acquired epidermolysis bullosa[1] |
| Specialty | Dermatology  |
Epidermolysis bullosa acquisita (EBA) 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
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[]
- ^ 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[]
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Categories:
- Chronic blistering cutaneous conditions
- Rare diseases
- Cutaneous condition stubs