Alp, H.Alp, E.Çimen, DeryaOran, B.2020-03-262020-03-2620101300-0381https://hdl.handle.net/20.500.12395/25625Greig cephalopolysyndactyly syndrome (GCPS) is an autosomal dominant condition characterized by distinct combination of craniofacial, hand and food malformations. It is caused by mutations of the gene GLI3, located on 7p13. The clinical features consistent with GCPS are typical craniofacial findings, post or preaxial polysyndactyly of the hands and feet. In this report we describe clinical and radiological findings of a Turkish family in which five members of three generations could be examined. Dysgenesis of the corpus callosum is diagnosed in one of the patients. A rare clinical manifestation, pectus excavatum, is also seen in two of the cases. Copyright © 2010 by Türkiye Klinikleri.eninfo:eu-repo/semantics/closedAccessFunnel chestGLI3 protein, humanPolydactylySyndactylyArticle1917479Q4