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Apparent Apert syndrome with polydactyly: rare pleiotropic manifestation or new syndrome?
1Unité de Recherchés de Génétique Médicale (INSERM U12 and CNRS UA 584), Hôpital des Enfants-Malades, Paris, France.
American Journal of Medical Genetics
|September 1, 1987
Abstract:
Two patients are described with a syndrome which resembles Apert syndrome with polydactyly of hands and feet. This association is apparently rare and we think that this may represent a distinct syndrome separate from Apert syndrome.