{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,26]],"date-time":"2026-09-26T02:43:58Z","timestamp":1790390638690,"version":"4.1.0"},"reference-count":28,"publisher":"Elsevier BV","issue":"5","license":[{"start":{"date-parts":[[2006,5,1]],"date-time":"2006-05-01T00:00:00Z","timestamp":1146441600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Optometry - Journal of the American Optometric Association"],"published-print":{"date-parts":[[2006,5]]},"DOI":"10.1016\/j.optm.2006.03.005","type":"journal-article","created":{"date-parts":[[2006,5,6]],"date-time":"2006-05-06T06:24:57Z","timestamp":1146896697000},"page":"217-222","source":"Crossref","is-referenced-by-count":39,"title":["Crouzon syndrome"],"prefix":"10.1016","volume":"77","author":[{"given":"Ernest L.","family":"Bowling","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Fernando D.","family":"Burstein","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.optm.2006.03.005_bib1","first-page":"545","article-title":"Dysostose cranio-faciale hereditaire","volume":"33","author":"Crouzon","year":"1912","journal-title":"Bull Mem Soc Med Hosp Paris"},{"issue":"2","key":"10.1016\/j.optm.2006.03.005_bib2","doi-asserted-by":"crossref","first-page":"87","DOI":"10.1016\/0039-6257(90)90067-6","article-title":"Congenital craniofacial anomalies of ophthalmic importance","volume":"35","author":"Fries","year":"1990","journal-title":"Surv Ophthalmol"},{"key":"10.1016\/j.optm.2006.03.005_bib3","first-page":"993","article-title":"Craniofacial dysostosis (Crouzon\u2019s disease) as a dominant hereditary affection","volume":"18","author":"Fogh-Andersen","year":"1943","journal-title":"Nord Med"},{"key":"10.1016\/j.optm.2006.03.005_bib4","doi-asserted-by":"crossref","first-page":"98","DOI":"10.1542\/peds.23.1.98","article-title":"Craniofacial dysostosis. Crouzon\u2019s disease","volume":"23","author":"Dodge","year":"1959","journal-title":"Pediatrics"},{"key":"10.1016\/j.optm.2006.03.005_bib5","series-title":"Congenital Anomalies of the Eye","first-page":"81","article-title":"Cranial dysostosis with pronounced digital impressions (pseudo-Crouzon dysostosis)","author":"Franceschetti","year":"1968"},{"issue":"1","key":"10.1016\/j.optm.2006.03.005_bib6","doi-asserted-by":"crossref","first-page":"18","DOI":"10.1111\/j.1525-1470.1996.tb01180.x","article-title":"Crouzon disease with acanthosis nigricans and melanocytic nevi","volume":"13","author":"Gines","year":"1996","journal-title":"Pediatr Dermatol"},{"issue":"Suppl","key":"10.1016\/j.optm.2006.03.005_bib7","first-page":"47","article-title":"The premature synostosis of the cranial sutures","volume":"5","author":"Bertelson","year":"1958","journal-title":"Arch Ophthalmol"},{"issue":"3","key":"10.1016\/j.optm.2006.03.005_bib8","doi-asserted-by":"crossref","first-page":"275","DOI":"10.1038\/ng1194-275","article-title":"Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2","volume":"8","author":"Jabs","year":"1994","journal-title":"Nat Genet"},{"issue":"Suppl","key":"10.1016\/j.optm.2006.03.005_bib9","doi-asserted-by":"crossref","first-page":"99","DOI":"10.1002\/ajmg.1320310514","article-title":"Craniosynostosis update 1987","volume":"4","author":"Cohen","year":"1988","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.optm.2006.03.005_bib10","doi-asserted-by":"crossref","first-page":"12","DOI":"10.1111\/j.1399-0004.1992.tb03620.x","article-title":"Birth prevalence studies of the Crouzon syndrome","volume":"41","author":"Cohen","year":"1992","journal-title":"Clin Genet"},{"issue":"6","key":"10.1016\/j.optm.2006.03.005_bib11","doi-asserted-by":"crossref","first-page":"1129","DOI":"10.1016\/j.ophtha.2004.12.037","article-title":"Ophthalmic sequelae of Crouzon syndrome","volume":"112","author":"Gray","year":"2005","journal-title":"Ophthalmology"},{"issue":"4","key":"10.1016\/j.optm.2006.03.005_bib12","doi-asserted-by":"crossref","first-page":"275","DOI":"10.3109\/02844319609056405","article-title":"Craniofacial dysostosis","volume":"30","author":"Jarund","year":"1996","journal-title":"Scand J Plast Reconstr Surg Hand Surg"},{"key":"10.1016\/j.optm.2006.03.005_bib13","doi-asserted-by":"crossref","first-page":"500","DOI":"10.1016\/0002-9394(52)91316-0","article-title":"Hereditary craniofacial dysplasia","volume":"35","author":"Pinkerton","year":"1952","journal-title":"Am J Ophthalmol"},{"key":"10.1016\/j.optm.2006.03.005_bib14","unstructured":"Chen H. Crouzon syndrome. eMedicine. Available at www.emedicine.com\/PED\/topic511.htm. Last accessed March 14, 2004."},{"key":"10.1016\/j.optm.2006.03.005_bib15","first-page":"137","article-title":"An etiologic and nosologic overview of craniosynostosis syndromes","volume":"11","author":"Cohen","year":"1975","journal-title":"Birth Defects"},{"key":"10.1016\/j.optm.2006.03.005_bib16","first-page":"697","article-title":"Craniofacial dysplasia associated with congenital cataracta, impairment of hearing and brachydactyly","volume":"62","author":"Erneyi","year":"1966","journal-title":"Am J Ophthalmol"},{"key":"10.1016\/j.optm.2006.03.005_bib17","doi-asserted-by":"crossref","first-page":"219","DOI":"10.1136\/jmg.31.3.219","article-title":"Crouzon Syndrome is not linked to craniosynostosis loci at 7p and 5qter","volume":"31","author":"Reardon","year":"1994","journal-title":"J Med Genet"},{"key":"10.1016\/j.optm.2006.03.005_bib18","doi-asserted-by":"crossref","first-page":"80","DOI":"10.1097\/00003226-199401000-00014","article-title":"Bilateral keratoconus in Crouzon\u2019s Syndrome","volume":"13","author":"Perlman","year":"1994","journal-title":"Cornea"},{"key":"10.1016\/j.optm.2006.03.005_bib19","doi-asserted-by":"crossref","first-page":"539","DOI":"10.1097\/00006534-199509000-00004","article-title":"Crouzon and Apert Syndromes. Intracranial volume measurements before and after cranio-orbital reshaping in childhood","volume":"96","author":"Posnick","year":"1995","journal-title":"Plast Reconstr Surg"},{"key":"10.1016\/j.optm.2006.03.005_bib20","doi-asserted-by":"crossref","first-page":"112","DOI":"10.1597\/1545-1569(1992)029<0112:CSMBOC>2.3.CO;2","article-title":"Craniofacial skeletal measurements based on computed tomography. Part I. Accuracy and reproducibility","volume":"29","author":"Waitzmann","year":"1992","journal-title":"Cleft Palate-Craniofac J"},{"key":"10.1016\/j.optm.2006.03.005_bib21","first-page":"141","article-title":"Bilateral keratoconus in Crouzon\u2019s Syndrome with unilateral acute hydrops","volume":"14","author":"Wolter","year":"1977","journal-title":"J Pediatr Ophthalmol"},{"key":"10.1016\/j.optm.2006.03.005_bib22","unstructured":"Miklaszewska M, Szybejko-Machaj G. Crouzon syndrome. eMedicine. Available at www.emedicine.com\/derm\/topic734.htm. Last accessed March 14, 2004."},{"key":"10.1016\/j.optm.2006.03.005_bib23","first-page":"410","article-title":"Crouzon Sendromu","volume":"22","author":"Basar","year":"1992","journal-title":"Turk Oftalmol Gaz"},{"issue":"2","key":"10.1016\/j.optm.2006.03.005_bib24","doi-asserted-by":"crossref","first-page":"173","DOI":"10.1038\/ng0295-173","article-title":"Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes","volume":"9","author":"Rutland","year":"1995","journal-title":"Nat Genet"},{"issue":"9","key":"10.1016\/j.optm.2006.03.005_bib25","doi-asserted-by":"crossref","first-page":"744","DOI":"10.1136\/jmg.33.9.744","article-title":"A recurrent mutation, ala391glu, in the transmembrane region of FGFR3 causes Crouzon syndrome and acanthosis nigricans","volume":"33","author":"Wilkes","year":"1996","journal-title":"J Med Genet"},{"key":"10.1016\/j.optm.2006.03.005_bib26","unstructured":"Jablonski S. Multiple Congenital Anomaly\/Mental Retardation (MCA\/MR) Syndromes. National Library of Medicine. Available at www.nlm.nih.gov\/mesh\/jablonski\/syndrome_main.html. Last accessed March 24, 2004."},{"issue":"3","key":"10.1016\/j.optm.2006.03.005_bib27","doi-asserted-by":"crossref","first-page":"334","DOI":"10.1002\/ajmg.1320560327","article-title":"Craniosynostoses","volume":"56","author":"Cohen","year":"1995","journal-title":"Am J Med Genet"},{"issue":"5","key":"10.1016\/j.optm.2006.03.005_bib28","doi-asserted-by":"crossref","first-page":"433","DOI":"10.1597\/1545-1569(2000)037<0433:TCDSCS>2.0.CO;2","article-title":"The craniofacial dysostosis syndromes","volume":"37","author":"Posnick","year":"2000","journal-title":"Cleft Palate Craniofac J"}],"container-title":["Optometry - Journal of the American Optometric Association"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1529183906002004?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1529183906002004?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2023,5,7]],"date-time":"2023-05-07T05:57:20Z","timestamp":1683439040000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1529183906002004"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2006,5]]},"references-count":28,"journal-issue":{"issue":"5","published-print":{"date-parts":[[2006,5]]}},"alternative-id":["S1529183906002004"],"URL":"https:\/\/doi.org\/10.1016\/j.optm.2006.03.005","relation":{},"ISSN":["1529-1839"],"issn-type":[{"value":"1529-1839","type":"print"}],"subject":[],"published":{"date-parts":[[2006,5]]}}}