{"title":"非典型Apert综合征:颅骨、面中部和下颌骨的顺序和节段性牵张成骨。","authors":"Nobuyuki Mitsukawa, Kaneshige Satoh, Takashi Hayashi, Tadashi Morishita, Yoshiaki Hosaka","doi":"10.1080/02844310701383993","DOIUrl":null,"url":null,"abstract":"<p><p>We describe a boy with Apert syndrome, including cranial deformities and syndactyly (acrocephalosyndactyly), though intracranial hypertension, exophthalmos, and midfacial hypoplasia were mild. We treated him by mandibular distraction, in addition to fronto-orbital distraction, and Le Fort III midfacial distraction, with good results.</p>","PeriodicalId":49569,"journal":{"name":"Scandinavian Journal of Plastic and Reconstructive Surgery and Hand Surgery","volume":"43 2","pages":"109-12"},"PeriodicalIF":0.0000,"publicationDate":"2009-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/02844310701383993","citationCount":"3","resultStr":"{\"title\":\"Atypical Apert syndrome: sequential and segmental distraction osteogenesis of the skull, midface, and mandible.\",\"authors\":\"Nobuyuki Mitsukawa, Kaneshige Satoh, Takashi Hayashi, Tadashi Morishita, Yoshiaki Hosaka\",\"doi\":\"10.1080/02844310701383993\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>We describe a boy with Apert syndrome, including cranial deformities and syndactyly (acrocephalosyndactyly), though intracranial hypertension, exophthalmos, and midfacial hypoplasia were mild. We treated him by mandibular distraction, in addition to fronto-orbital distraction, and Le Fort III midfacial distraction, with good results.</p>\",\"PeriodicalId\":49569,\"journal\":{\"name\":\"Scandinavian Journal of Plastic and Reconstructive Surgery and Hand Surgery\",\"volume\":\"43 2\",\"pages\":\"109-12\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2009-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1080/02844310701383993\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Scandinavian Journal of Plastic and Reconstructive Surgery and Hand Surgery\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1080/02844310701383993\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Scandinavian Journal of Plastic and Reconstructive Surgery and Hand Surgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/02844310701383993","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3
摘要
我们描述了一个患有Apert综合征的男孩，包括颅骨畸形和并指畸形(肢头并指畸形)，尽管颅内高压，突出眼和面中发育不全是轻微的。除额眶牵张外，我们对他进行下颌牵张和Le Fort III型面中牵张治疗，效果良好。
Atypical Apert syndrome: sequential and segmental distraction osteogenesis of the skull, midface, and mandible.
We describe a boy with Apert syndrome, including cranial deformities and syndactyly (acrocephalosyndactyly), though intracranial hypertension, exophthalmos, and midfacial hypoplasia were mild. We treated him by mandibular distraction, in addition to fronto-orbital distraction, and Le Fort III midfacial distraction, with good results.
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