Vohwinkel syndrome: ichthyosiform variant in a family
An. bras. dermatol
; An. bras. dermatol;93(5): 723-725, Sept.-Oct. 2018. graf
Article
de En
| LILACS
| ID: biblio-949938
Bibliothèque responsable:
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.
Mots clés
Texte intégral:
1
Indice:
LILACS
Sujet Principal:
Malformations multiples
/
Anomalies morphologiques congénitales de la main
/
Kératose palmoplantaire
/
Surdité neurosensorielle
/
Ichtyose
Limites du sujet:
Child, preschool
/
Humans
/
Male
langue:
En
Texte intégral:
An. bras. dermatol
Thème du journal:
DERMATOLOGIA
Année:
2018
Type:
Article