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dc.contributor.authorReinehr, Clarissa Prieto Hermanpt_BR
dc.contributor.authorPeruzzo, Julianopt_BR
dc.contributor.authorCestari, Tania Ferreirapt_BR
dc.date.accessioned2019-10-10T03:49:31Zpt_BR
dc.date.issued2018pt_BR
dc.identifier.issn0365-0596pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/200345pt_BR
dc.description.abstractVohwinkel 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.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofAnais brasileiros de dermatologia. Vol. 93, no. 5 (2018), p. 723-725pt_BR
dc.rightsOpen Accessen
dc.subjectGenetic diseases, inbornen
dc.subjectIctiosept_BR
dc.subjectIchthyosisen
dc.subjectDermatopatias genéticaspt_BR
dc.subjectCeratodermia palmar e plantarpt_BR
dc.subjectKeratinocytesen
dc.subjectDoenças genéticas inataspt_BR
dc.subjectKeratoderma, palmoplantaren
dc.subjectSkin diseases, geneticen
dc.subjectCriançapt_BR
dc.subjectRelatos de casospt_BR
dc.titleVohwinkel syndrome : ichthyosiform variant in a familypt_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb001102504pt_BR
dc.type.originNacionalpt_BR


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