[Multiple eccrine hydrocystomas of the eyelids in the framework of Schöpf syndrome. A case report]

Autor: C, Dot, M, Dordain, E, Boucher, F, Metge, P, Millet, M, Maille, J, Maurin
Jazyk: francouzština
Rok vydání: 2000
Předmět:
Zdroj: Journal francais d'ophtalmologie. 23(8)
ISSN: 0181-5512
Popis: Schöpf-Schultz-Passarge syndrome is a rare ectodermal dysplasia described by Schöpf in 1971. The disease is characterized by hypodontia, hypotrichosis, palmoplantar keratoderma, hypoplastic nails and eyelid hydrocystomas. We report the case of a 71-year-old man, the first French description of this syndrome, who remarkably presented all the signs. The patient also had skin tumors, multiple eccrime hidrocystomas and aspectific macular degeneration. A review of the literature is discussed.
Databáze: OpenAIRE