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Characteristics of children with Netherton syndrome: a review of 21 patients.
Prodinger, C; Yerlett, N; MacDonald, C; Subhanitthaya, C; Laimer, M; Goh, L; Du Toit, G; Mellerio, J E; Petrof, G; Martinez, A E.
Afiliação
  • Prodinger C; Department of Dermatology and Allergology, University Hospital of the Paracelsus Medical University, Salzburg, Austria.
  • Yerlett N; Dietetics Department, Great Ormond Street Hospital for Children, NHS Foundation Trust, London, UK.
  • MacDonald C; Department of Dermatology, Great Ormond Street Hospital for Children, NHS Foundation Trust, London, UK.
  • Subhanitthaya C; Department of Dermatology, Great Ormond Street Hospital for Children, NHS Foundation Trust, London, UK.
  • Laimer M; Department of Dermatology and Allergology, University Hospital of the Paracelsus Medical University, Salzburg, Austria.
  • Goh L; Paediatric Allergy Clinic, University College London Hospital NHS Foundation Trust, London, UK.
  • Du Toit G; Children's Allergy Service, Evelina Children's Hospital, Guy's and St. Thomas's NHS Foundation Trust, London, UK.
  • Mellerio JE; St. John's Institute of Dermatology, King's College London, Guy's Hospital NHS Foundation Trust, London, UK.
  • Petrof G; Department of Dermatology, Great Ormond Street Hospital for Children, NHS Foundation Trust, London, UK.
  • Martinez AE; Department of Dermatology, Great Ormond Street Hospital for Children, NHS Foundation Trust, London, UK.
J Eur Acad Dermatol Venereol ; 35(7): e466-e469, 2021 Jul.
Article em En | MEDLINE | ID: mdl-33725371

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Eritrodermia Ictiosiforme Congênita / Síndrome de Netherton Tipo de estudo: Diagnostic_studies Limite: Child / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Eritrodermia Ictiosiforme Congênita / Síndrome de Netherton Tipo de estudo: Diagnostic_studies Limite: Child / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article