Serdar Ozturk, Ismail Sahin, Unsal Coskun, Ilhami Surer, Mustafa Sengezer
{"title":"复直肠尾侧退缩综合征所致缺损的闭合。","authors":"Serdar Ozturk, Ismail Sahin, Unsal Coskun, Ilhami Surer, Mustafa Sengezer","doi":"10.1080/02844310701682923","DOIUrl":null,"url":null,"abstract":"<p><p>Caudal regression syndrome covers a range of congenital malformations that range from simple anal atresia to absence of sacral, lumbar, and possibly lower thoracic, vertebrae. To the best of our knowledge, this is the first case of caudal regression syndrome combined with rectal duplication. We present a case and describe our technique of reconstruction.</p>","PeriodicalId":49569,"journal":{"name":"Scandinavian Journal of Plastic and Reconstructive Surgery and Hand Surgery","volume":"43 6","pages":"343-5"},"PeriodicalIF":0.0000,"publicationDate":"2009-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/02844310701682923","citationCount":"0","resultStr":"{\"title\":\"Closure of the defect resulting from caudal regression syndrome with duplicated rectum.\",\"authors\":\"Serdar Ozturk, Ismail Sahin, Unsal Coskun, Ilhami Surer, Mustafa Sengezer\",\"doi\":\"10.1080/02844310701682923\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Caudal regression syndrome covers a range of congenital malformations that range from simple anal atresia to absence of sacral, lumbar, and possibly lower thoracic, vertebrae. To the best of our knowledge, this is the first case of caudal regression syndrome combined with rectal duplication. We present a case and describe our technique of reconstruction.</p>\",\"PeriodicalId\":49569,\"journal\":{\"name\":\"Scandinavian Journal of Plastic and Reconstructive Surgery and Hand Surgery\",\"volume\":\"43 6\",\"pages\":\"343-5\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2009-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1080/02844310701682923\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Scandinavian Journal of Plastic and Reconstructive Surgery and Hand Surgery\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1080/02844310701682923\",\"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/10.1080/02844310701682923","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Closure of the defect resulting from caudal regression syndrome with duplicated rectum.
Caudal regression syndrome covers a range of congenital malformations that range from simple anal atresia to absence of sacral, lumbar, and possibly lower thoracic, vertebrae. To the best of our knowledge, this is the first case of caudal regression syndrome combined with rectal duplication. We present a case and describe our technique of reconstruction.