{"title":"尾侧退化综合征1例报告","authors":"A. Karaman","doi":"10.5505/JKARTALTR.2014.60320","DOIUrl":null,"url":null,"abstract":"Caudal regression syndrome is a rare congenital anomaly , which results from a developmental failure of the caudal mesoderm during the fetal period. We present a case of caudal regression syndrome composed of a spectrum of anomalies including sirenomelia , dysplasia of the lower lumbar vertebrae , sacrum , coccyx and pelvic bones , genitouri nary and anorectal anomalies , and dysplasia of the lung , as seen during infantography and MR lmagmg.","PeriodicalId":22729,"journal":{"name":"The Journal of Kartal Training and Research Hospital","volume":"27 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2015-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Caudal Regression Syndrome: A Case Report\",\"authors\":\"A. Karaman\",\"doi\":\"10.5505/JKARTALTR.2014.60320\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Caudal regression syndrome is a rare congenital anomaly , which results from a developmental failure of the caudal mesoderm during the fetal period. We present a case of caudal regression syndrome composed of a spectrum of anomalies including sirenomelia , dysplasia of the lower lumbar vertebrae , sacrum , coccyx and pelvic bones , genitouri nary and anorectal anomalies , and dysplasia of the lung , as seen during infantography and MR lmagmg.\",\"PeriodicalId\":22729,\"journal\":{\"name\":\"The Journal of Kartal Training and Research Hospital\",\"volume\":\"27 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2015-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Journal of Kartal Training and Research Hospital\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5505/JKARTALTR.2014.60320\",\"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 Journal of Kartal Training and Research Hospital","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5505/JKARTALTR.2014.60320","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Caudal regression syndrome is a rare congenital anomaly , which results from a developmental failure of the caudal mesoderm during the fetal period. We present a case of caudal regression syndrome composed of a spectrum of anomalies including sirenomelia , dysplasia of the lower lumbar vertebrae , sacrum , coccyx and pelvic bones , genitouri nary and anorectal anomalies , and dysplasia of the lung , as seen during infantography and MR lmagmg.