John Libbey Eurotext




Delleman syndrome: report of a case with a mild phenotype
European Journal of Dermatology. Volume 10, Number 8, 623-6, December 2000, Cas cliniques
Free Article
Author(s) : S. Cambiaghi, P. Savant Levet, G. Guala, D. Baldini, R. Gianotti
Summary : 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.
Keywords : abnormalities, multiple skin abnormalities, skin neoplasms, eye abnormalities, aplasia cutis.

Delleman syndrome: report of a case with a mild phenotype