S. S. Hahn, Y. Hahn, Y. Hahn, K. W. Choi, B. Min, O. J. Kim
{"title":"杜宾-约翰逊综合征1例。","authors":"S. S. Hahn, Y. Hahn, Y. Hahn, K. W. Choi, B. Min, O. J. Kim","doi":"10.12701/YUJM.2002.19.1.68","DOIUrl":null,"url":null,"abstract":"Dubin-Johnson syndrome is a form of benign, familial idiopathic jaundice presenting with chronic intermittent conjugated hyperbilirubinemia and a melanin-like pigment has been found in the parenchymal liver cells. This disorder is rarely diagnosed in the neonatal period. We report a case of Dubin-Johnson syndrome presenting with neonatal cholestasis.","PeriodicalId":83948,"journal":{"name":"Taehan Uihak Hyophoe chi. The Journal of the Korean Medical Association","volume":"23 1","pages":"609-14"},"PeriodicalIF":0.0000,"publicationDate":"2002-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"[A case of Dubin-Johnson syndrome].\",\"authors\":\"S. S. Hahn, Y. Hahn, Y. Hahn, K. W. Choi, B. Min, O. J. Kim\",\"doi\":\"10.12701/YUJM.2002.19.1.68\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Dubin-Johnson syndrome is a form of benign, familial idiopathic jaundice presenting with chronic intermittent conjugated hyperbilirubinemia and a melanin-like pigment has been found in the parenchymal liver cells. This disorder is rarely diagnosed in the neonatal period. We report a case of Dubin-Johnson syndrome presenting with neonatal cholestasis.\",\"PeriodicalId\":83948,\"journal\":{\"name\":\"Taehan Uihak Hyophoe chi. The Journal of the Korean Medical Association\",\"volume\":\"23 1\",\"pages\":\"609-14\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2002-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Taehan Uihak Hyophoe chi. The Journal of the Korean Medical Association\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.12701/YUJM.2002.19.1.68\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Taehan Uihak Hyophoe chi. The Journal of the Korean Medical Association","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.12701/YUJM.2002.19.1.68","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Dubin-Johnson syndrome is a form of benign, familial idiopathic jaundice presenting with chronic intermittent conjugated hyperbilirubinemia and a melanin-like pigment has been found in the parenchymal liver cells. This disorder is rarely diagnosed in the neonatal period. We report a case of Dubin-Johnson syndrome presenting with neonatal cholestasis.
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