Congenital absence of the skin secondary to the self-improving subtype of dystrophic epidermolysis bullosa with recurrent lesions throughout early childhood.

Dean, Owen; Cusick, Elizabeth H; Grover, Raminder; Mercurio, Mary G; Richardson, Christopher T

Dean, Owen; Cusick, Elizabeth H; Grover, Raminder; Mercurio, Mary G; Richardson, Christopher T.

Afiliação

Dean O; University of Rochester School of Medicine and Dentistry, Rochester, New York.
Cusick EH; Department of Dermatology, University of Rochester Medical Center, Rochester, New York.
Grover R; Beutner Laboratories, Buffalo, New York.
Mercurio MG; Department of Dermatology, University of Rochester Medical Center, Rochester, New York.
Richardson CT; Department of Dermatology, University of Rochester Medical Center, Rochester, New York.

JAAD Case Rep ; 7: 137-140, 2021 Jan.

Article em En | MEDLINE | ID: mdl-33426254

Palavras-chave

Bart syndrome; CAS, congenital absence of the skin; EB, epidermolysis bullosa; SI-DEB, self-improving subtype of dystrophic epidermolysis bullosa; aplasia cutis congenita type VI; bullous dermolysis of the newborn; congenital absence of the skin; dystrophic epidermolysis bullosa; pediatric dermatology; subtype self-improving

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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article