{"title":"胎儿畸形1例报告及产前诊断探讨","authors":"D. Pandey, Pragati Divedi, P. Mishra, P. Mishra","doi":"10.4103/2278-960X.140095","DOIUrl":null,"url":null,"abstract":"Sirenomelia is a rare polymalformative, lethal congenital anomaly, characterized by fusion of both lower limbs, bilateral renal agenesis, absent external genitalia, aberrant fetal vasculature, and severe oligohydramnios. We hereby report a case of Sirenomelia diagnosed postnatally in an unbooked pregnancy presenting at the thirty‑fifth gestational week. Keywords: Diabetes mellitus, dysmorphic lower limb, prenatal diagnosis, sirenomelia","PeriodicalId":356195,"journal":{"name":"Journal of Basic and Clinical Reproductive Sciences","volume":"6 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2014-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"4","resultStr":"{\"title\":\"Sirenomelia: Case report and discussion of its prenatal diagnosis\",\"authors\":\"D. Pandey, Pragati Divedi, P. Mishra, P. Mishra\",\"doi\":\"10.4103/2278-960X.140095\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Sirenomelia is a rare polymalformative, lethal congenital anomaly, characterized by fusion of both lower limbs, bilateral renal agenesis, absent external genitalia, aberrant fetal vasculature, and severe oligohydramnios. We hereby report a case of Sirenomelia diagnosed postnatally in an unbooked pregnancy presenting at the thirty‑fifth gestational week. Keywords: Diabetes mellitus, dysmorphic lower limb, prenatal diagnosis, sirenomelia\",\"PeriodicalId\":356195,\"journal\":{\"name\":\"Journal of Basic and Clinical Reproductive Sciences\",\"volume\":\"6 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2014-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"4\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Basic and Clinical Reproductive Sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4103/2278-960X.140095\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Basic and Clinical Reproductive Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/2278-960X.140095","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Sirenomelia: Case report and discussion of its prenatal diagnosis
Sirenomelia is a rare polymalformative, lethal congenital anomaly, characterized by fusion of both lower limbs, bilateral renal agenesis, absent external genitalia, aberrant fetal vasculature, and severe oligohydramnios. We hereby report a case of Sirenomelia diagnosed postnatally in an unbooked pregnancy presenting at the thirty‑fifth gestational week. Keywords: Diabetes mellitus, dysmorphic lower limb, prenatal diagnosis, sirenomelia
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