| Revista: | Anais brasileiros de dermatologia |
| Base de datos: | PERIÓDICA |
| Número de sistema: | 000410474 |
| ISSN: | 0365-0596 |
| Autors: | Sanches, Sarah1 Rebellato, Priscila Regina Orso1 Fabre, Andrea Buosi1 Campos, Giovana Liz Marioto de1 |
| Institucions: | 1Faculdade Evangelica do Parana, Hospital Universitario Evangelico de Curitiba, Curitiba, Parana. Brasil |
| Any: | 2017 |
| Període: | May-Jun |
| Volum: | 92 |
| Número: | 3 |
| Paginació: | 417-418 |
| País: | Brasil |
| Idioma: | Inglés |
| Tipo de documento: | Artículo |
| Enfoque: | Caso clínico |
| Resumen en inglés | Ectodermal dysplasias are conditions that present primary defects in two or more tissues of ectodermal origin and can be classified as hypohidrotic and hidrotic. Hidrotic ectodermal dysplasia or Clouston syndrome is an autosomal dominant genodermatosis and appears as a triad of clinical findings: palmoplantar keratoderma, nail dystrophy, and hypotrichosis. The hair is sparse and brittle. The nails become thickened and dystrophic, which is an essential characteristic of the syndrome. The diagnosis is made based on clinical findings. This study reports a case of a patient who began with changes in hair, nails and palmoplantar keratoderma in early childhood |
| Disciplines | Medicina |
| Paraules clau: | Dermatología, Diagnóstico, Genética, Síndrome de Clouston, Genodermatosis, Queratodermia plantar, Displasia ectodérmica, Hipotricosis |
| Keyword: | Medicine, Dermatology, Diagnosis, Genetics, Clouston syndrome, Genodermatosis, Plantar keratodermia, Ectodermal dysplasia, Hypotrichosis |
| Text complet: | Texto completo (Ver HTML) |
