A Rare Cause of Hypokalemia: Gitelman Syndrome
Full Text (PDF)
Mehmet Ali Eren 1, Suzan Tabur 1, Burcu Sezgin 1, Tevfik Sabuncu 1
More Detail
1 Harran University, Faculty of Medicine, Division of Endocrinology, Department of Internal Medicine, Şanlıurfa, Turkey

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 of the patients had been closed.

Keywords

License

This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Article Type: Case Report

EUR J GEN MED, 2011, Volume 8, Issue 2, 154-156

https://doi.org/10.29333/ejgm/82719

Publication date: 11 Apr 2011

Article Views: 1473

Article Downloads: 1343

Open Access References How to cite this article