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Vohwinkel syndrome: ichthyosiform variant in a family
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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Dermatologia
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6106675/ https://www.ncbi.nlm.nih.gov/pubmed/30156625 http://dx.doi.org/10.1590/abd1806-4841.20187440 |
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author | Reinehr, Clarissa Prieto Herman Peruzzo, Juliano Cestari, Tania |
author_facet | Reinehr, Clarissa Prieto Herman Peruzzo, Juliano Cestari, Tania |
author_sort | Reinehr, Clarissa Prieto Herman |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6106675 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Sociedade Brasileira de Dermatologia |
record_format | MEDLINE/PubMed |
spelling | pubmed-61066752018-09-01 Vohwinkel syndrome: ichthyosiform variant in a family Reinehr, Clarissa Prieto Herman Peruzzo, Juliano Cestari, Tania An Bras Dermatol Case Report 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. Sociedade Brasileira de Dermatologia 2018 /pmc/articles/PMC6106675/ /pubmed/30156625 http://dx.doi.org/10.1590/abd1806-4841.20187440 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivative License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium provided the original work is properly cited and the work is not changed in any way. |
spellingShingle | Case Report Reinehr, Clarissa Prieto Herman Peruzzo, Juliano Cestari, Tania Vohwinkel syndrome: ichthyosiform variant in a family |
title | Vohwinkel syndrome: ichthyosiform variant in a family |
title_full | Vohwinkel syndrome: ichthyosiform variant in a family |
title_fullStr | Vohwinkel syndrome: ichthyosiform variant in a family |
title_full_unstemmed | Vohwinkel syndrome: ichthyosiform variant in a family |
title_short | Vohwinkel syndrome: ichthyosiform variant in a family |
title_sort | vohwinkel syndrome: ichthyosiform variant in a family |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6106675/ https://www.ncbi.nlm.nih.gov/pubmed/30156625 http://dx.doi.org/10.1590/abd1806-4841.20187440 |
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