Delleman syndrome: report of a case with a mild phenotype.
Eur J Dermatol
; 10(8): 623-6, 2000 Dec.
Article
em En
| MEDLINE
| ID: mdl-11125327
ABSTRACT
Delleman syndrome is a rare disorder characterised by orbital cysts, micro/anophthalmia, malformations of the central nervous system, focal aplasia cutis, and multiple skin appendages (oculocerebrocutaneous syndrome). Although cutaneous findings provide the main clues for the diagnosis, the syndrome has received little attention in the dermatological literature. A new case of oculocerebrocutaneous syndrome with predominant and typical cutaneous involvement is reported.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Anormalidades da Pele
/
Neoplasias Cutâneas
/
Anormalidades Múltiplas
/
Sistema Nervoso Central
/
Anormalidades do Olho
Tipo de estudo:
Diagnostic_studies
/
Observational_studies
/
Prognostic_studies
Limite:
Humans
/
Male
/
Newborn
Idioma:
En
Revista:
Eur J Dermatol
Assunto da revista:
DERMATOLOGIA
Ano de publicação:
2000
Tipo de documento:
Article
País de afiliação:
Itália