{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,30]],"date-time":"2026-04-30T04:37:01Z","timestamp":1777523821835,"version":"3.51.4"},"reference-count":22,"publisher":"SAGE Publications","issue":"8","license":[{"start":{"date-parts":[[2022,3,30]],"date-time":"2022-03-30T00:00:00Z","timestamp":1648598400000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["The Cleft Palate Craniofacial Journal"],"published-print":{"date-parts":[[2023,8]]},"abstract":"<jats:p>Saethre-Chotzen syndrome (SCS) is a known craniosynostosis syndrome with a variable presentation of craniofacial and somatic involvement. Congenital coronal craniosynostosis is most commonly observed in SCS; however, progressive postnatal craniosynostosis of other sutures has been reported. The authors present 2 infants with progressive postnatal craniosynostosis and SCS caused by chromosome 7p deletions including the TWIST1 gene. The evolution of their clinical features and a literature review of patients with syndromic, postnatal progressive craniosynostosis illustrate the importance of longitudinal observation and management of these patients.<\/jats:p>","DOI":"10.1177\/10556656221090844","type":"journal-article","created":{"date-parts":[[2022,3,31]],"date-time":"2022-03-31T01:30:31Z","timestamp":1648690231000},"page":"1021-1028","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":3,"title":["Postnatal Progressive Craniosynostosis in Syndromic Conditions: Two Patients With Saethre-Chotzen Due to\n                    <i>TWIST1<\/i>\n                    Gene Deletions and Review of the Literature"],"prefix":"10.1177","volume":"60","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-2455-4011","authenticated-orcid":false,"given":"Rama J","family":"Alawneh","sequence":"first","affiliation":[{"name":"Faculty of Medicine, King Abdullah University Hospital, Jordan University of Science and Technology, Irbid, Jordan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Andrea L","family":"Johnson","sequence":"additional","affiliation":[{"name":"Department of Cellular Biology and Molecular Genetics, University of Maryland College Park, College Park, MD, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Julie Elizabeth","family":"Hoover-Fong","sequence":"additional","affiliation":[{"name":"Greenberg Center for Skeletal Dysplasias, Department of Genetic Medicine, Johns Hopkins University, Baltimore, MD, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Eric M","family":"Jackson","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, MD, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jordan P","family":"Steinberg","sequence":"additional","affiliation":[{"name":"Division of Plastic 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