History, Diagnosis, Pathogenesis, and Nomenclature in Sublamina Densa-Type Linear IgA Disease

Author:

Hashimoto Takashi1,Yamagami Jun2,Zone John J.3

Affiliation:

1. Department of Dermatology, Osaka City University Graduate School of Medicine, Osaka, Japan

2. Department of Dermatology, Keio University School of Medicine, Tokyo, Japan

3. Department of Dermatology, University of Utah School of Medicine, Salt Lake City

Publisher

American Medical Association (AMA)

Subject

Dermatology

Reference7 articles.

1. Evaluation and comparison of clinical and laboratory characteristics of patients with IgA epidermolysis bullosa acquisita, linear IgA bullous dermatosis, and IgG epidermolysis bullosa acquisita.;Becker;JAMA Dermatol

2. Diagnostic significance of the immunofluorescent pattern in dermatitis herpetiformis.;Chorzelski;Int J Dermatol,1975

3. Immunoelectronmicroscopic localization of IgA in skin of patients with dermatitis herpetiformis.;Yaoita;J Invest Dermatol,1976

4. The 97 kDa linear IgA bullous disease antigen is identical to a portion of the extracellular domain of the 180 kDa bullous pemphigoid antigen, BPAg2.;Zone;J Invest Dermatol,1998

5. Type VII collagen is the major autoantigen for sublamina densa-type linear IgA bullous dermatosis.;Tsuchisaka;J Invest Dermatol,2015

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