Gitelman증후군 1예A Case of Gitelman Syndrome
- Other Titles
- A Case of Gitelman Syndrome
- Authors
- 한유진; 연은경; 김영창
- Issue Date
- 2012
- Publisher
- 순천향의학연구소
- Keywords
- Gitelman’s syndrome; Hypokalemia; Hypomagnesemia
- Citation
- Soonchunhyang Medical Science, v.18, no.2, pp 145 - 147
- Pages
- 3
- Journal Title
- Soonchunhyang Medical Science
- Volume
- 18
- Number
- 2
- Start Page
- 145
- End Page
- 147
- URI
- https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/15556
- ISSN
- 2233-4289
- 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.
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Collections - College of Medicine > Department of Medical Education > 1. Journal Articles
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