Epidermolysis Bullosa Acquisita Develops in Dominant Dystrophic Epidermolysis Bullosa

J Invest Dermatol. 2016 Jan;136(1):320-3. doi: 10.1038/JID.2015.370.

Authors

Ryota Hayashi¹, Ken Natsuga², Mika Watanabe², Hiroaki Iwata², Satoru Shinkuma², Akiko Ito¹, Yukiko Masui¹, Masaaki Ito¹, Yutaka Shimomura³

Affiliations

¹ Division of Dermatology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
² Department of Dermatology, Hokkaido University Graduate School of Medicine, Sapporo, Japan.
³ Division of Dermatology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan; Laboratory of Genetic Skin Diseases, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan. Electronic address: yshimo@med.niigata-u.ac.jp.

PMID: 26763454
DOI: 10.1038/JID.2015.370

No abstract available

Publication types

Letter
Research Support, Non-U.S. Gov't

MeSH terms

Adult
Age Factors
Biopsy, Needle
Cell Transdifferentiation / physiology*
Child
Collagen Type VII / genetics*
Epidermolysis Bullosa Acquisita / immunology
Epidermolysis Bullosa Acquisita / pathology*
Epidermolysis Bullosa Acquisita / physiopathology
Epidermolysis Bullosa Dystrophica / genetics*
Epidermolysis Bullosa Dystrophica / pathology*
Epidermolysis Bullosa Dystrophica / physiopathology
Female
Humans
Immunohistochemistry
Japan
Male
Middle Aged
Pedigree
Risk Assessment
Severity of Illness Index
Sex Factors

Substances

COL7A1 protein, human
Collagen Type VII