Familial Graham-Little-Picardi-Lassueur syndrome across 3 generations.

Soto-García, Diego; Feal-Cortizas, Carlos; Álvarez, Carlos; Couselo-Rodríguez, Carmen; Martínez-Fernández, Sandra; Flórez, Ángeles

Soto-García, Diego; Feal-Cortizas, Carlos; Álvarez, Carlos; Couselo-Rodríguez, Carmen; Martínez-Fernández, Sandra; Flórez, Ángeles.

Afiliação

Soto-García D; Dermatología inflamatoria, pediátrica y oncológica Research Group, Galicia Sur Health Research Institute (Instituto Investigación Sanitaria Galicia Sur), SERGAS-UVIGO, Vigo, Spain.
Feal-Cortizas C; Department of Dermatology, University Hospital of Pontevedra, Pontevedra, Spain.
Álvarez C; Dermatología inflamatoria, pediátrica y oncológica Research Group, Galicia Sur Health Research Institute (Instituto Investigación Sanitaria Galicia Sur), SERGAS-UVIGO, Vigo, Spain.
Couselo-Rodríguez C; Department of Dermatology, University Hospital of Pontevedra, Pontevedra, Spain.
Martínez-Fernández S; Dermatología inflamatoria, pediátrica y oncológica Research Group, Galicia Sur Health Research Institute (Instituto Investigación Sanitaria Galicia Sur), SERGAS-UVIGO, Vigo, Spain.
Flórez Á; Department of Pathology, University Hospital of Pontevedra, Pontevedra, Spain.

JAAD Case Rep ; 23: 128-132, 2022 May.

Article em En | MEDLINE | ID: mdl-35495969

Palavras-chave

GLPLS, Graham-Little-Piccardi-Lassueur syndrome; HLA, human leukocyte antigen; LPP, lichen planopilaris; familial Graham-Little-Piccardi-Lassueur syndrome; lichen planopilaris; scarring alopecia

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: JAAD Case Rep Ano de publicação: 2022 Tipo de documento: Article

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: JAAD Case Rep Ano de publicação: 2022 Tipo de documento: Article