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، جلد ۶، شماره ۱، صفحات ۲۰-۲۴
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| عنوان فارسی |
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| چکیده فارسی مقاله |
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| کلیدواژه‌های فارسی مقاله |
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| عنوان انگلیسی |
Rare presentation of Gitelman syndrome: a case report and literature review |
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| چکیده انگلیسی مقاله |
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 history. She experienced an episode of tonic-clonic seizure, generalized muscle weakness, and severe hyponatremia as the first presentation of GS. The interesting point of this case was her late-onset presentation and the long period of her disease diagnosis; thus, it highlights the importance of considering this diagnosis. |
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| کلیدواژه‌های انگلیسی مقاله |
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| نویسندگان مقاله |
| Nasim Khajavirad
Department of Internal Medicine, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
| Saeed Shakiba
Department of Internal Medicine, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
| Mahsa Abbaszadeh
Department of Internal Medicine, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
| Sahar Karimpour Reyhan
Department of Internal Medicine, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
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| نشانی اینترنتی |
https://crcp.tums.ac.ir/index.php/crcp/article/view/352 |
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