{"title":"Klippel-Feil综合症。与斯普伦格尔畸形、动椎骨和其他骨骼、血液和呼吸系统疾病有不寻常的联系。一份病例报告。","authors":"A Greenspan, J Cohen, R M Szabo","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>An unusual presentation of Klippel-Feil syndrome prompts a detailed description of this anomaly and a review of the literature. The patient, a six-year-old boy, had, in addition, multiple associated congenital anomalies that included Sprengel deformity, omovertebral bone, scoliosis, hypoplasia of the right thumb, plagiocephaly, choanal atresia, and Diamond-Blackfan anemia.</p>","PeriodicalId":77501,"journal":{"name":"Bulletin of the Hospital for Joint Diseases Orthopaedic Institute","volume":"51 1","pages":"54-62"},"PeriodicalIF":0.0000,"publicationDate":"1991-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Klippel-Feil syndrome. An unusual association with Sprengel deformity, omovertebral bone, and other skeletal, hematologic, and respiratory disorders. A case report.\",\"authors\":\"A Greenspan, J Cohen, R M Szabo\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>An unusual presentation of Klippel-Feil syndrome prompts a detailed description of this anomaly and a review of the literature. The patient, a six-year-old boy, had, in addition, multiple associated congenital anomalies that included Sprengel deformity, omovertebral bone, scoliosis, hypoplasia of the right thumb, plagiocephaly, choanal atresia, and Diamond-Blackfan anemia.</p>\",\"PeriodicalId\":77501,\"journal\":{\"name\":\"Bulletin of the Hospital for Joint Diseases Orthopaedic Institute\",\"volume\":\"51 1\",\"pages\":\"54-62\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1991-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Bulletin of the Hospital for Joint Diseases Orthopaedic Institute\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bulletin of the Hospital for Joint Diseases Orthopaedic Institute","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Klippel-Feil syndrome. An unusual association with Sprengel deformity, omovertebral bone, and other skeletal, hematologic, and respiratory disorders. A case report.
An unusual presentation of Klippel-Feil syndrome prompts a detailed description of this anomaly and a review of the literature. The patient, a six-year-old boy, had, in addition, multiple associated congenital anomalies that included Sprengel deformity, omovertebral bone, scoliosis, hypoplasia of the right thumb, plagiocephaly, choanal atresia, and Diamond-Blackfan anemia.