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 language | English |
|---|---|
| Pages (from-to) | 623-626 |
| Number of pages | 4 |
| Journal | European Journal of Dermatology |
| Volume | 10 |
| Issue number | 8 |
| Publication status | Published - 2000 |
Keywords
- Abnormalities
- Aplasia cutis
- Eye abnormalities
- Multiple skin abnormalities
- Skin neoplasms
ASJC Scopus subject areas
- Dermatology
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Cite this
Cambiaghi, S., Savant Levet, P., Guala, G., Baldini, D., & Gianotti, R. (2000). Delleman syndrome: Report of a case with a mild phenotype. European Journal of Dermatology, 10(8), 623-626.