Facial deformity in Crouzon syndrome is characterized by exophthalmos, exorbitism, mild hypertelorism, and maxillary hypoplasia with a Class III occlusion. The Göteborg craniofacial unit corrects this deformity in selected patients by the 2-stage procedure of "spectaclesplasty" followed by a Le Fort I maxillary osteotomy at skeletal maturity. "Spectacles" is a reference to the bilateral circumf...

Crouzon syndrome is a rare craniofacial dysostosis with autosomal dominant mode of inheritance with variable phenotypic expression .It is characterized by early closure of cranial sutures leading to range of problems like calvarial deformities, midface hypoplasia and exopthalmus. Early diagnosis is critical in these cases to avoid complications like hearing and vision problems.There are 50% cha...

A family study was based on 184 consecutive patients who had undergone surgery for craniosynostosis at The Hospital for Sick Children, London, between 1953 and 1976. Of these, 127 were traced and visited and are the probands for this study. Crouzon syndrome was recognised in 16, Apert in 11, Saethre-Chotzen in nine, and Pfeiffer in two. In addition, two probands had Saethre-Chotzen-like facies ...