Vohwinkel syndrome: ichthyosiform variant in a family
An. bras. dermatol
; 93(5): 723-725, Sept.-Oct. 2018. graf
Article
em En
| LILACS
| ID: biblio-949938
Biblioteca responsável:
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.
Palavras-chave
Texto completo:
1
Índice:
LILACS
Assunto principal:
Anormalidades Múltiplas
/
Deformidades Congênitas da Mão
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Ceratodermia Palmar e Plantar
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Perda Auditiva Neurossensorial
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Ictiose
Limite:
Child, preschool
/
Humans
/
Male
Idioma:
En
Revista:
An. bras. dermatol
Assunto da revista:
DERMATOLOGIA
Ano de publicação:
2018
Tipo de documento:
Article