{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,6]],"date-time":"2026-02-06T05:40:10Z","timestamp":1770356410340,"version":"3.49.0"},"reference-count":32,"publisher":"Journal of Neurosurgery Publishing Group (JNSPG)","issue":"3","license":[{"start":{"date-parts":[[2021,1,18]],"date-time":"2021-01-18T00:00:00Z","timestamp":1610928000000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2021,1,18]]},"abstract":"<jats:sec>\n                    <jats:title>BACKGROUND<\/jats:title>\n                    <jats:p>Squamosal sutures are minor sutures of the human skull. Early isolated fusion of the sutures (squamosal synostosis) is rarely found.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>OBSERVATIONS<\/jats:title>\n                    <jats:p>The authors report a case of a girl who presented with an abnormal head shape and bilateral squamosal synostosis. Genetic testing revealed a chromosome 1p12\u20131p13.3 deletion. She has been managed with conservative treatment of the synostosis. She has global developmental delay and multiple anomalies due to the chromosome abnormality.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>LESSONS<\/jats:title>\n                    <jats:p>Isolated squamosal suture synostosis could be an uncommon feature of chromosome 1p12\u20131p13.3 deletion.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.3171\/case20102","type":"journal-article","created":{"date-parts":[[2021,1,29]],"date-time":"2021-01-29T15:32:36Z","timestamp":1611934356000},"source":"Crossref","is-referenced-by-count":1,"title":["Bilateral squamosal synostosis: unusual presentation of chromosome 1p12\u20131p13.3 deletion. Illustrative case"],"prefix":"10.3171","volume":"1","author":[{"given":"Sarut","family":"Chaisrisawadisuk","sequence":"first","affiliation":[{"name":"Division of Plastic Surgery, Department of Surgery, and"},{"name":"Cleft and Craniofacial South Australia, Women\u2019s and Children\u2019s Hospital, North Adelaide, South Australia, Australia; and"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nithiwat","family":"Vatanavicharn","sequence":"additional","affiliation":[{"name":"Division of Medical Genetics, Department of Paediatrics, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand;"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Verayuth","family":"Praphanphoj","sequence":"additional","affiliation":[{"name":"Medical Genetics Center, Sai Mai District, Bangkok, Thailand;"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Peter J.","family":"Anderson","sequence":"additional","affiliation":[{"name":"Cleft and Craniofacial South Australia, Women\u2019s and Children\u2019s Hospital, North Adelaide, South Australia, Australia; and"},{"name":"Faculty of Health and Medical Sciences, University of Adelaide, Adelaide, South Australia, Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mark H.","family":"Moore","sequence":"additional","affiliation":[{"name":"Cleft and Craniofacial South Australia, Women\u2019s and Children\u2019s Hospital, North Adelaide, South Australia, Australia; and"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"1754","reference":[{"issue":"5","key":"b1","series-title":"J Craniofac Surg","doi-asserted-by":"publisher","first-page":"1547","DOI":"10.1097\/SCS.0b013e3181ebe62f","article-title":"Craniosynostosis involving the squamous temporal sutures: a rare and possibly underreported etiology for cranial vault asymmetry","volume":"21","author":"Ranger A","year":"2010","unstructured":"Ranger A, Chaudhary N, Matic D. 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