Acral peeling skin syndrome resulting from a novel homozygous mutation in the CSTA gene-A report of two cases.

Sarika, Georgina-Maria; Ibrahim, Ruba; Zlotogorski, Abraham; Molho-Pessach, Vered

Sarika, Georgina-Maria; Ibrahim, Ruba; Zlotogorski, Abraham; Molho-Pessach, Vered.

Afiliação

Sarika GM; Department of Dermatology, The Faculty of Medicine, Hadassah Medical Center, Hebrew University of Jerusalem, Jerusalem, Israel.
Ibrahim R; Department of Dermatology, The Faculty of Medicine, Hadassah Medical Center, Hebrew University of Jerusalem, Jerusalem, Israel.
Zlotogorski A; Department of Dermatology, The Faculty of Medicine, Hadassah Medical Center, Hebrew University of Jerusalem, Jerusalem, Israel.
Molho-Pessach V; Department of Dermatology, The Faculty of Medicine, Hadassah Medical Center, Hebrew University of Jerusalem, Jerusalem, Israel.

Pediatr Dermatol ; 38(6): 1546-1548, 2021 Nov.

Article em En | MEDLINE | ID: mdl-34713485

Assuntos

Mutação; Humanos; Dermatopatias/congênito

Palavras-chave

CSTA; acral peeling skin syndrome; cystatin A; exfoliative ichthyosis

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Mutação Limite: Humans Idioma: En Revista: Pediatr Dermatol Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Israel

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