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KMID : 1214920120180020145
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Soonchunhyang Medical Science
2012 Volume.18 No. 2 p.145 ~ p.147
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A Case of Gitelman Syndrome
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Han Yu-Jin
Yeon Eun-Kyeong
Kim Young-Chang
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Abstract
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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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KEYWORD
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Gitelman’s syndrome, Hypokalemia, Hypomagnesemia
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Listed journal information
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