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It involves the premature fusion of sutures of the cranial vault, base, orbital and maxillary region. The clinical presentation of this congenital deformity depends on the pattern and timing of sutural fusion. The present report describes the features and management of this syndrome in an 18-year-old woman. The patient presented with a hypoplastic maxilla, deficient midface, exorbitism due to shallow orbits, severe crowding and bilateral crossbite. A multidisciplinary approach involving orthodontics and surgical intervention with distraction osteogenesis brought about marked improvement in the facial profile, occlusion and upper airway. The aesthetics and function were greatly enhanced, and the results were found to be stable at the end of three years. <\/jats:p>","DOI":"10.1177\/14653125211019412","type":"journal-article","created":{"date-parts":[[2021,6,11]],"date-time":"2021-06-11T00:35:41Z","timestamp":1623371741000},"page":"71-78","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":7,"title":["Comprehensive management of Crouzon syndrome: A case report with three-year follow-up"],"prefix":"10.1177","volume":"49","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-2352-9743","authenticated-orcid":false,"given":"Tulika","family":"Tripathi","sequence":"first","affiliation":[{"name":"Department of Orthodontics and Dentofacial Orthopedics, Maulana Azad Institute of Dental Sciences, New Delhi, India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Dhirendra","family":"Srivastava","sequence":"additional","affiliation":[{"name":"Oral and 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