{"title":"新生儿空肠闭锁1例","authors":"Muhammet Mesut Nezir Engin","doi":"10.33169/gsoaoj-i-105","DOIUrl":null,"url":null,"abstract":"Jejunal atresia is a rare congenital malformation. Mortality, which was 90% in the 1950s, decreased to approximately 10%. There are studies reporting 1/5000 incidence. We presented a case with polyhydramnios and enlargement of the intestines in the prenatal period, a nutritional defect after birth, with dilated bowel loops with air-fluid levels on the direct abdominal x-ray, and operated on the first day of postnatal diagnosis.","PeriodicalId":119444,"journal":{"name":"General Surgery Open Access Open Journa","volume":"60 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2020-06-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Jejunal Atresia in Newborn: A Case Report\",\"authors\":\"Muhammet Mesut Nezir Engin\",\"doi\":\"10.33169/gsoaoj-i-105\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Jejunal atresia is a rare congenital malformation. Mortality, which was 90% in the 1950s, decreased to approximately 10%. There are studies reporting 1/5000 incidence. We presented a case with polyhydramnios and enlargement of the intestines in the prenatal period, a nutritional defect after birth, with dilated bowel loops with air-fluid levels on the direct abdominal x-ray, and operated on the first day of postnatal diagnosis.\",\"PeriodicalId\":119444,\"journal\":{\"name\":\"General Surgery Open Access Open Journa\",\"volume\":\"60 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-06-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"General Surgery Open Access Open Journa\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.33169/gsoaoj-i-105\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"General Surgery Open Access Open Journa","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.33169/gsoaoj-i-105","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Jejunal atresia is a rare congenital malformation. Mortality, which was 90% in the 1950s, decreased to approximately 10%. There are studies reporting 1/5000 incidence. We presented a case with polyhydramnios and enlargement of the intestines in the prenatal period, a nutritional defect after birth, with dilated bowel loops with air-fluid levels on the direct abdominal x-ray, and operated on the first day of postnatal diagnosis.
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