Epidermolysis bullosa acquisita: current diagnosis and therapy
Epidermolysis bullosa acquisita (EBA) is an acquired, autoimmune subepidermal blistering disease with an approximate prevalence of 0,2/million people. The hallmark of EBA is the presence of autoantibodies (mainly IgG class) to anchoring fibril collagen (type VII collagen) located at the dermal-epide...
Main Authors: | Christine R. Mehren, Robert Gniadecki |
---|---|
Format: | Article |
Language: | English |
Published: |
PAGEPress Publications
2011-11-01
|
Series: | Dermatology Reports |
Subjects: | |
Online Access: | http://www.pagepress.org/journals/index.php/dr/article/view/2476 |
Similar Items
-
Diagnostic value of elastic fibers staining in dystrophic epidermolysis bullosa
by: Min-tong HE, et al.
Published: (2020-04-01) -
IgM-mediated epidermolysis bullosa acquisita
by: Sidney Harrison, BS, et al.
Published: (2024-04-01) -
Epidermolysis bullosa acquisita
by: V. V. Chikin, et al.
Published: (2017-08-01) -
Epidermolysis bullosa acquisita: diagnostic difficulties
by: Izabela Staniszewska, et al.
Published: (2024-02-01) -
Utility of Immunofluorescence Antigen Mapping in Hereditary Epidermolysis Bullosa
by: Raghavendra Rao, et al.
Published: (2021-01-01)