Lentiginosis and café-au-lait macules as part of the phenotypic spectrum of PAX3-related disorders.

Morice-Picard, F; Letertre, O; Lasseaux, E; Cario-Andre, M; Arveiler, B; Taieb, A

Morice-Picard, F; Letertre, O; Lasseaux, E; Cario-Andre, M; Arveiler, B; Taieb, A.

Afiliação

Morice-Picard F; Department of Dermatology and Pediatric Dermatology, National Reference Centre for Rare Disorders, Centre Hospitalier Universitaire du Bordeaux, Bordeaux, France.
Letertre O; Department of Dermatology and Pediatric Dermatology, National Reference Centre for Rare Disorders, Centre Hospitalier Universitaire du Bordeaux, Bordeaux, France.
Lasseaux E; Department of Medical Genetics, Bordeaux University Hospital, Bordeaux, France.
Cario-Andre M; Department of Dermatology and Pediatric Dermatology, National Reference Centre for Rare Disorders, Centre Hospitalier Universitaire du Bordeaux, Bordeaux, France.
Arveiler B; Department of Medical Genetics, Bordeaux University Hospital, Bordeaux, France.
Taieb A; Department of Dermatology and Pediatric Dermatology, National Reference Centre for Rare Disorders, Centre Hospitalier Universitaire du Bordeaux, Bordeaux, France.

Clin Exp Dermatol ; 45(5): 621-623, 2020 Jul.

Article em En | MEDLINE | ID: mdl-32086958

Assuntos

Manchas Café com Leite/genética; Lentigo/genética; Mutação; Fator de Transcrição PAX3/genética; Fenótipo; Adulto; Manchas Café com Leite/patologia; Criança; Feminino; Heterozigoto; Humanos; Lentigo/patologia; Masculino; Pele/patologia

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Manchas Café com Leite / Fator de Transcrição PAX3 / Lentigo / Mutação Limite: Adult / Child / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article

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