Vohwinkel syndrome : ichthyosiform variant in a family
dc.contributor.author | Reinehr, Clarissa Prieto Herman | pt_BR |
dc.contributor.author | Peruzzo, Juliano | pt_BR |
dc.contributor.author | Cestari, Tania Ferreira | pt_BR |
dc.date.accessioned | 2019-10-10T03:49:31Z | pt_BR |
dc.date.issued | 2018 | pt_BR |
dc.identifier.issn | 0365-0596 | pt_BR |
dc.identifier.uri | http://hdl.handle.net/10183/200345 | pt_BR |
dc.description.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. | en |
dc.format.mimetype | application/pdf | pt_BR |
dc.language.iso | eng | pt_BR |
dc.relation.ispartof | Anais brasileiros de dermatologia. Vol. 93, no. 5 (2018), p. 723-725 | pt_BR |
dc.rights | Open Access | en |
dc.subject | Genetic diseases, inborn | en |
dc.subject | Ictiose | pt_BR |
dc.subject | Ichthyosis | en |
dc.subject | Dermatopatias genéticas | pt_BR |
dc.subject | Ceratodermia palmar e plantar | pt_BR |
dc.subject | Keratinocytes | en |
dc.subject | Doenças genéticas inatas | pt_BR |
dc.subject | Keratoderma, palmoplantar | en |
dc.subject | Skin diseases, genetic | en |
dc.subject | Criança | pt_BR |
dc.subject | Relatos de casos | pt_BR |
dc.title | Vohwinkel syndrome : ichthyosiform variant in a family | pt_BR |
dc.type | Artigo de periódico | pt_BR |
dc.identifier.nrb | 001102504 | pt_BR |
dc.type.origin | Nacional | pt_BR |
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