A Rare Cause of Hypokalemia: Gitelman Syndrome
Mehmet Ali Eren, Suzan Tabur, Burcu Sezgin, Tevfik Sabuncu
Abstract
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Mehmet Ali Eren, Suzan Tabur, Burcu Sezgin, Tevfik Sabuncu
Abstract
Open-access reader
Gitelman syndrome is a rare, inherited disorder. Hypokalemia, metabolic alkalosis, hypomagnesemia and hypocalciuria are the characteristic abnormalities of this syndrome. This syndrome can lead to growth retardation and to rarely serious complications such as paralysis and cardiac arrest. Therefore, early recognition and treatment are important. In this paper we reported a young adulthood with classic Gitelman syndrome. Electrolyte imbalances were resolved with treatment; however, further growth wasn’t achieved since the epiphyses of the patients had been closed.
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Gitelman syndrome is a rare, inherited disorder. Hypokalemia, metabolic alkalosis, hypomagnesemia and hypocalciuria are the characteristic abnormalities of this syndrome. This syndrome can lead to growth retardation and to rarely serious complications such as paralysis and cardiac arrest. Therefore, early recognition and treatment are important. In this paper we reported a young adulthood with classic Gitelman syndrome. Electrolyte imbalances were resolved with treatment; however, further growth wasn’t achieved since the epiphyses of the patients had been closed.
Key concepts: Hypocalciuria, Hypokalemia, Gitelman syndrome, Hypomagnesemia, Metabolic alkalosis, Medicine, Internal medicine, Electrolyte Disorder