{"title":"偶然发现的吉特尔曼综合征。","authors":"M B Leonard, D Neithercut","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Gitelman's syndrome is characterised by hypokalaemia, hypomagnesaemia and tetany. This rare disorder is not well described in the literature, probably due to its similarity with Bartter's syndrome. We describe the symptoms and treatment of a young patient whom we consider to have Gitelman's syndrome.</p>","PeriodicalId":22312,"journal":{"name":"The British journal of clinical practice","volume":"51 2","pages":"121-4"},"PeriodicalIF":0.0000,"publicationDate":"1997-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"An incidental finding of Gitelman's syndrome.\",\"authors\":\"M B Leonard, D Neithercut\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Gitelman's syndrome is characterised by hypokalaemia, hypomagnesaemia and tetany. This rare disorder is not well described in the literature, probably due to its similarity with Bartter's syndrome. We describe the symptoms and treatment of a young patient whom we consider to have Gitelman's syndrome.</p>\",\"PeriodicalId\":22312,\"journal\":{\"name\":\"The British journal of clinical practice\",\"volume\":\"51 2\",\"pages\":\"121-4\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1997-03-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The British journal of clinical practice\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The British journal of clinical practice","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Gitelman's syndrome is characterised by hypokalaemia, hypomagnesaemia and tetany. This rare disorder is not well described in the literature, probably due to its similarity with Bartter's syndrome. We describe the symptoms and treatment of a young patient whom we consider to have Gitelman's syndrome.
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