Data di Pubblicazione:
2000
Citazione:
Delleman syndrome : report of a case with a mild phenotype / S. Cambiaghi, P.S. Levet, G. Guala, D. Baldini, R. Gianotti. - In: EUROPEAN JOURNAL OF DERMATOLOGY. - ISSN 1167-1122. - 10:8(2000 Dec), pp. 623-626.
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.
Tipologia IRIS:
01 - Articolo su periodico
Keywords:
abnormalities, multiple; central nervous system; eye abnormalities; follow-up studies; humans; infant, newborn; male; phenotype; skin abnormalities; skin neoplasms; syndrome
Elenco autori:
S. Cambiaghi, P.S. Levet, G. Guala, D. Baldini, R. Gianotti
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