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Congenital ichthyosiform erythroderma with epidermolysis due to a novel frameshift mutation in KRT10.
Kurz, Bernadett; Koschitzki, Kevin-Thomas; Hehr, Ute; Germer, Ute; Schreml, Julia; Langhammer, Florian; Schreml, Stephan.
Afiliación
  • Kurz B; Department of Dermatology, University Hospital Regensburg, Regensburg, Germany.
  • Koschitzki KT; Department of Dermatology, University Hospital Regensburg, Regensburg, Germany.
  • Hehr U; Institute of Human Genetics, University Hospital Regensburg, Regensburg, Germany.
  • Germer U; Department of Gynecology and Obstetrics, Caritas Hospital St. Josef, Regensburg, Germany.
  • Schreml J; Institute of Human Genetics, University Hospital of Cologne, Cologne, Germany.
  • Langhammer F; Department of Neonatology, University Children's Hospital Regensburg (KUNO), Hospital St. Hedwig of the Order of St. John, University Hospital Regensburg, Regensburg, Germany.
  • Schreml S; Department of Dermatology, University Hospital Regensburg, Regensburg, Germany.
JAAD Case Rep ; 35: 74-76, 2023 May.
Article en En | MEDLINE | ID: mdl-37101807
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: JAAD Case Rep Año: 2023 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Estados Unidos
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: JAAD Case Rep Año: 2023 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Estados Unidos