Delleman syndrome: Report of a case with a mild phenotype

S. Cambiaghi, P. Savant Levet, G. Guala, D. Baldini, R. Gianotti

Research output: Contribution to journalArticle

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.

Original languageEnglish
Pages (from-to)623-626
Number of pages4
JournalEuropean Journal of Dermatology
Volume10
Issue number8
Publication statusPublished - 2000

Keywords

  • Abnormalities
  • Aplasia cutis
  • Eye abnormalities
  • Multiple skin abnormalities
  • Skin neoplasms

ASJC Scopus subject areas

  • Dermatology

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