Rare presentation of Gitelman syndrome: a case report and literature review
Gitelman Syndrome (GS), also known as familial hypokalemia-hypomagnesemia, is a rare genetic disorder. GS presents with a specific defect in kidney function, that leads to hypokalemia, hypomagnesemia, metabolic alkalosis, and hypocalciuria. Here, we present a 30-year-old woman without a medical hist...
Main Authors: | Nasim Khajavirad, Saeed Shakiba, Mahsa Abbaszadeh, Sahar Karimpour Reyhan |
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Format: | Article |
Language: | English |
Published: |
Tehran University of Medical Sciences
2021-05-01
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Series: | Case Reports in Clinical Practice |
Subjects: | |
Online Access: | https://crcp.tums.ac.ir/index.php/crcp/article/view/352 |
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