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Hidrocystomes eccrines multiples des paupieres dans le cadre du syndrome de Schopf A propos d'un cas Dot C; Dordain M; Boucher E; Metge F; Millet P; Maille M; Maurin JJ Fr Ophtalmol 2000[Oct]; 23 (8): 809-16Schopf-Schultz-Passarge syndrome is a rare ectodermal dysplasia described by Schopf 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.|Aged[MESH]|Anodontia/*diagnosis[MESH]|Eccrine Glands/*pathology[MESH]|Eyelid Diseases/*diagnosis[MESH]|Humans[MESH]|Hypotrichosis/*diagnosis[MESH]|Keratoderma, Palmoplantar/*diagnosis[MESH]|Male[MESH]|Nail Diseases/diagnosis[MESH]|Skin Neoplasms/diagnosis[MESH]|Syndrome[MESH] |
