scholarly journals Epidermolysis bullosa acquisita and anti-p200 pemphigoid as major subepidermal autoimmune bullous diseases diagnosed by floor binding on indirect immunofluorescence microscopy using human salt-split skin

2017 ◽  
Vol 83 (5) ◽  
pp. 550 ◽  
Author(s):  
Raghavendra Rao ◽  
Nupur Goyal ◽  
ShrutakirthiD Shenoi ◽  
Sathish Pai ◽  
Pramod Kumar ◽  
...  
Keyword(s):  
Indirect Immunofluorescence ◽  
Epidermolysis Bullosa ◽  
Immunofluorescence Microscopy ◽  
Epidermolysis Bullosa Acquisita ◽  
Indirect Immunofluorescence Microscopy ◽  
Autoimmune Bullous Diseases ◽  
Bullous Diseases ◽  
Split Skin

Autoimmune bullous diseases

2020 ◽  
pp. 5612-5620
Author(s):  
Kathy Taghipour ◽  
Fenella Wojnarowska
Keyword(s):  
Basement Membrane ◽  
Basal Cell ◽  
Epidermolysis Bullosa ◽  
Cell Layer ◽  
Basement Membrane Zone ◽  
Epidermolysis Bullosa Acquisita ◽  
Significant Morbidity ◽  
Heterogenous Group ◽  
Autoimmune Bullous Diseases ◽  
Bullous Diseases

Autoimmune bullous diseases of the skin are a heterogenous group of blistering diseases that affect the skin and/or mucosal membranes. They are associated with significant morbidity and mortality and may present to several different specialists. They are broadly divided into two groups depending on the location of the blisters formed in the skin, which may be subepidermal (pemphigoids, linear IgA disease, dermatitis herpetiformis, epidermolysis bullosa acquisita) or intraepidermal (pemphigus group). Pathogenic autoantibodies (IgG, IgA) target either the proteins that provide keratinocyte adhesion (intraepidermal disease) or the proteins of hemidesmosomes that attach the basal cell layer to the basement membrane zone (subepidermal disease).

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