{"title":"新生儿色素失禁1例","authors":"N. Ekneligoda, T. Perera, R. Prashana","doi":"10.4038/sljpm.v1i1.28","DOIUrl":null,"url":null,"abstract":"Incontinentia pigmenti (IP) is a rare neuroectodermal dysplasia with an estimated incidence of 0.7 cases per 100,000 births. Up to date approximately 1,200 cases have been reported in scientific literature. IP has a multisystemic involvement where the skin manifestations are the hall mark and could be seen even at birth. We present a baby girl with typical skin manifestations of IP seen at birth.","PeriodicalId":273627,"journal":{"name":"Sri Lanka Journal of Perinatal Medicine","volume":"43 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2020-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A Case of Incontinentia Pigmenti in a New Born\",\"authors\":\"N. Ekneligoda, T. Perera, R. Prashana\",\"doi\":\"10.4038/sljpm.v1i1.28\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Incontinentia pigmenti (IP) is a rare neuroectodermal dysplasia with an estimated incidence of 0.7 cases per 100,000 births. Up to date approximately 1,200 cases have been reported in scientific literature. IP has a multisystemic involvement where the skin manifestations are the hall mark and could be seen even at birth. We present a baby girl with typical skin manifestations of IP seen at birth.\",\"PeriodicalId\":273627,\"journal\":{\"name\":\"Sri Lanka Journal of Perinatal Medicine\",\"volume\":\"43 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Sri Lanka Journal of Perinatal Medicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4038/sljpm.v1i1.28\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Sri Lanka Journal of Perinatal Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4038/sljpm.v1i1.28","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Incontinentia pigmenti (IP) is a rare neuroectodermal dysplasia with an estimated incidence of 0.7 cases per 100,000 births. Up to date approximately 1,200 cases have been reported in scientific literature. IP has a multisystemic involvement where the skin manifestations are the hall mark and could be seen even at birth. We present a baby girl with typical skin manifestations of IP seen at birth.
求助内容：
应助结果提醒方式：
京公网安备 11010802042870号
