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Vohwinkel syndrome: ichthyosiform variant in a family
Reinehr, Clarissa Prieto Herman; Peruzzo, Juliano; Cestari, Tania.
Affiliation
  • Reinehr, Clarissa Prieto Herman; Universidade Federal do Rio Grande do Sul. Program of Post-graduation in Medical Sciences. Porto Alegre. BR
  • Peruzzo, Juliano; Universidade Federal do Rio Grande do Sul. Hospital de Clínicas de Porto Alegre. Department of Dermatology. Porto Alegre. BR
  • Cestari, Tania; Universidade Federal do Rio Grande do Sul. Hospital de Clínicas de Porto Alegre. Department of Dermatology. Porto Alegre. BR
An. bras. dermatol ; An. bras. dermatol;93(5): 723-725, Sept.-Oct. 2018. graf
Article de En | LILACS | ID: biblio-949938
Bibliothèque responsable: BR1.1
ABSTRACT
Abstract Vohwinkel syndrome belongs to the group of hereditary palmoplantar keratoderma, having an autosomal dominant inheritance. In this report, the authors present a case of a four-year-old boy with diffuse scaling over his entire body and transgredient palmoplantar hyperkeratosis with some fissured areas. Family evaluation revealed that his mother and other family members were affected. Based on his clinical findings and on family history, the diagnosis of the ichthyotic Vohwinkel syndrome subtype, characterized by generalized ichthyosis and palmoplantar hyperkeratosis, was established.
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Texte intégral: 1 Indice: LILACS Sujet Principal: Malformations multiples / Anomalies morphologiques congénitales de la main / Kératose palmoplantaire / Surdité neurosensorielle / Ichtyose Limites du sujet: Child, preschool / Humans / Male langue: En Texte intégral: An. bras. dermatol Thème du journal: DERMATOLOGIA Année: 2018 Type: Article

Texte intégral: 1 Indice: LILACS Sujet Principal: Malformations multiples / Anomalies morphologiques congénitales de la main / Kératose palmoplantaire / Surdité neurosensorielle / Ichtyose Limites du sujet: Child, preschool / Humans / Male langue: En Texte intégral: An. bras. dermatol Thème du journal: DERMATOLOGIA Année: 2018 Type: Article