{"title":"Agnathia及相关畸形1例报告。","authors":"D M Brown, J L Marsh","doi":"10.1597/1545-1569(1990)027<0415:aaamac>2.3.co;2","DOIUrl":null,"url":null,"abstract":"<p><p>A case of a rare first branchial arch anomaly with severe hypoplasia of the mandible and fusion between the mandible and adjacent bones is presented. The patient also had intracranial, cardiac, and acral deformities. The craniofacial malformations may reflect incomplete separation of the first branchial arch into its maxillary and mandibular processes. The association between the craniofacial and other corporal anomalies is unknown.</p>","PeriodicalId":76622,"journal":{"name":"The Cleft palate journal","volume":"27 4","pages":"415-8"},"PeriodicalIF":0.0000,"publicationDate":"1990-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1597/1545-1569(1990)027<0415:aaamac>2.3.co;2","citationCount":"32","resultStr":"{\"title\":\"Agnathia and associated malformations: a case report.\",\"authors\":\"D M Brown, J L Marsh\",\"doi\":\"10.1597/1545-1569(1990)027<0415:aaamac>2.3.co;2\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>A case of a rare first branchial arch anomaly with severe hypoplasia of the mandible and fusion between the mandible and adjacent bones is presented. The patient also had intracranial, cardiac, and acral deformities. The craniofacial malformations may reflect incomplete separation of the first branchial arch into its maxillary and mandibular processes. The association between the craniofacial and other corporal anomalies is unknown.</p>\",\"PeriodicalId\":76622,\"journal\":{\"name\":\"The Cleft palate journal\",\"volume\":\"27 4\",\"pages\":\"415-8\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1990-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1597/1545-1569(1990)027<0415:aaamac>2.3.co;2\",\"citationCount\":\"32\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Cleft palate journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1597/1545-1569(1990)027<0415:aaamac>2.3.co;2\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Cleft palate journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1597/1545-1569(1990)027<0415:aaamac>2.3.co;2","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Agnathia and associated malformations: a case report.
A case of a rare first branchial arch anomaly with severe hypoplasia of the mandible and fusion between the mandible and adjacent bones is presented. The patient also had intracranial, cardiac, and acral deformities. The craniofacial malformations may reflect incomplete separation of the first branchial arch into its maxillary and mandibular processes. The association between the craniofacial and other corporal anomalies is unknown.