Gitelman증후군 1예
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 한유진 | - |
dc.contributor.author | 연은경 | - |
dc.contributor.author | 김영창 | - |
dc.date.accessioned | 2021-08-12T03:47:18Z | - |
dc.date.available | 2021-08-12T03:47:18Z | - |
dc.date.issued | 2012 | - |
dc.identifier.issn | 2233-4289 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/15556 | - |
dc.description.abstract | Gitelman’s syndrome is an autosomal recessive disorder characterized by hypokalemic metabolic alkalosis, hypomagnesemia, and hypocalciuria that has recently been reported to be linked to thiazide-sensitive Na-Cl cotransporter gene mutation. We have experienced one patient whose initial complaint was paresthesia of hand and feet, who had hypokalemic metabolic alkalosis, hypomagnesemia,and hypocalciuria. We report the case of Gitelman’s syndrome with a brief review of related literature. | - |
dc.format.extent | 3 | - |
dc.language | 한국어 | - |
dc.language.iso | KOR | - |
dc.publisher | 순천향의학연구소 | - |
dc.title | Gitelman증후군 1예 | - |
dc.title.alternative | A Case of Gitelman Syndrome | - |
dc.type | Article | - |
dc.publisher.location | 대한민국 | - |
dc.identifier.bibliographicCitation | Soonchunhyang Medical Science, v.18, no.2, pp 145 - 147 | - |
dc.citation.title | Soonchunhyang Medical Science | - |
dc.citation.volume | 18 | - |
dc.citation.number | 2 | - |
dc.citation.startPage | 145 | - |
dc.citation.endPage | 147 | - |
dc.identifier.kciid | ART001734982 | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | kciCandi | - |
dc.subject.keywordAuthor | Gitelman’s syndrome | - |
dc.subject.keywordAuthor | Hypokalemia | - |
dc.subject.keywordAuthor | Hypomagnesemia | - |
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