A rare cause of hypokalemia: Gitelman syndrome

3Citations
Citations of this article
5Readers
Mendeley users who have this article in their library.

Abstract

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 ofthe patients had been closed.

Cite

CITATION STYLE

APA

Eren, M. A., Tabur, S., Sezgin, B., & Sabuncu, T. (2011). A rare cause of hypokalemia: Gitelman syndrome. European Journal of General Medicine, 8(2), 154–156. https://doi.org/10.29333/ejgm/82719

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free