{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,6]],"date-time":"2026-06-06T19:14:35Z","timestamp":1780773275389,"version":"3.54.1"},"reference-count":20,"publisher":"SAGE Publications","issue":"1","license":[{"start":{"date-parts":[[2021,2,12]],"date-time":"2021-02-12T00:00:00Z","timestamp":1613088000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/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":[[2022,1]]},"abstract":"<jats:p>\n                    Campomelic dysplasia (CMPD) is a skeletal disorder resulting from\n                    <jats:italic>SOX9<\/jats:italic>\n                    gene mutations. Palatoplasty is rare due to a high lethality rate in infants from respiratory distress. Our patient had characteristic symptoms of CMPD, including short bowed limbs, macrocephaly, low-set ears, short palpebral fissures, hypertelorism, a flat nasal bridge, a long philtrum, micrognathia, and a cleft palate. We performed a Furlow palatoplasty when the patient was 2 years 9 months of age, after respiratory conditions had stabilized. We reviewed the literature of CMPD cases that underwent palatoplasty and discussed the optimal timing and surgical methods.\n                  <\/jats:p>","DOI":"10.1177\/1055665621992654","type":"journal-article","created":{"date-parts":[[2021,2,12]],"date-time":"2021-02-12T06:04:33Z","timestamp":1613109873000},"page":"132-136","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":2,"title":["Palatoplasty for the Patient With Campomelic Dysplasia\u2014Report of a Case and Review of the Literature"],"prefix":"10.1177","volume":"59","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-2193-7105","authenticated-orcid":false,"given":"Kaya","family":"Narimatsu","sequence":"first","affiliation":[{"name":"Department of Dentistry and Oral Surgery, Nagaoka Red Cross Hospital, Nagaoka city, Niigata, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-7264-2120","authenticated-orcid":false,"given":"Akihiko","family":"Iida","sequence":"additional","affiliation":[{"name":"Department of Dentistry and Oral Surgery, Nagaoka Red Cross Hospital, Nagaoka city, Niigata, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-5826-6616","authenticated-orcid":false,"given":"Takanori","family":"Kobayashi","sequence":"additional","affiliation":[{"name":"Department of Dentistry and Oral Surgery, Nagaoka Red Cross Hospital, Nagaoka city, Niigata, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"179","published-online":{"date-parts":[[2021,2,12]]},"reference":[{"key":"e_1_3_2_2_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.ajoms.2018.07.007"},{"key":"e_1_3_2_3_1","first-page":"53","article-title":"Genetical and clinical aspects of campomelic dysplasia","volume":"104","author":"Beluffi G","year":"1983","unstructured":"Beluffi G, Fraccaro M. 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