[Skip to Content]
Access to paid content on this site is currently suspended due to excessive activity being detected from your IP address 54.87.114.118. Please contact the publisher to request reinstatement.
[Skip to Content Landing]
Article
May 1989

Epidermolysis Bullosa Simplex SuperficialisA New Variant of Epidermolysis Bullosa Characterized by Subcorneal Skin Cleavage Mimicking Peeling Skin Syndrome

Author Affiliations

From the Department of Dermatology, School of Medicine (Drs Fine and Johnson), and Department of Pediatric Dentistry, School of Dentistry (Dr Wright), University of Alabama at Birmingham, and Dermatology Section, Medical Service, Birmingham (Ala) Veterans Administration Medical Center (Dr Fine).

Arch Dermatol. 1989;125(5):633-638. doi:10.1001/archderm.1989.01670170047006
Abstract

• We report a new variant of epidermolysis bullosa simplex (EBS), termed EBS superficialis, which is characterized by the development of skin cleavage just beneath the level of stratum corneum. In two of seven patients identified, a second and more focal cleft within the lower third of the epidermis was also detected. Epidermolysis bullosa simplex superficialis appears to be transmitted as an autosomal dominant trait. It differs from other autosomal dominant forms of EBS by the common findings of milia and atrophic scarring, as well as involvement of oral and/or ocular surfaces. Epidermolysis bullosa simplex superficialis is further differentiated from peeling skin syndrome by the presence of blisters and the absence of spontaneous continual exfoliation or peeling.

(Arch Dermatol. 1989;125:633-638)

×