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Vohwinkel syndrome: ichthyosiform variant in a family.
Reinehr, Clarissa Prieto Herman; Peruzzo, Juliano; Cestari, Tania.
Affiliation
  • Reinehr CPH; Program of Post-graduation in Medical Sciences, Universidade Federal do Rio Grande do Sul, Porto Alegre (RS), Brazil.
  • Peruzzo J; Department of Dermatology, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande do Sul, Porto Alegre (RS), Brazil.
  • Cestari T; Department of Dermatology, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande do Sul, Porto Alegre (RS), Brazil.
An Bras Dermatol ; 93(5): 723-725, 2018.
Article in En | MEDLINE | ID: mdl-30156625
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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Hand Deformities, Congenital / Keratoderma, Palmoplantar / Hearing Loss, Sensorineural / Ichthyosis Limits: Child, preschool / Humans / Male Language: En Journal: An Bras Dermatol Year: 2018 Document type: Article Affiliation country: Brazil Country of publication: Spain

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Hand Deformities, Congenital / Keratoderma, Palmoplantar / Hearing Loss, Sensorineural / Ichthyosis Limits: Child, preschool / Humans / Male Language: En Journal: An Bras Dermatol Year: 2018 Document type: Article Affiliation country: Brazil Country of publication: Spain