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Gitelman syndrome presenting with hypomagnesemia, hypokalemia and hypocalciuria - A case report
2019
Journal:  
Medeniyet Medical Journal
Author:  
DOI:  
10.5222/MMJ.2019.39000
Abstract:

Gitelman syndrome is a rare renal tubulopathy characterized by inherited autosomal recessive, hypokalemic metabolic alkalosis with hypomagnesemia and hypocalciuria. The diagnosis of Gitelman syndrome is usually established during adolescence, but is also observed in childhood and even in the adulthood period. In this case report, we presented a 19-year-old male patient who was diagnosed as Gitelman Syndrome and admitted to the hospital with symptoms of muscle weakness, cramps and weakness.

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Medeniyet Medical Journal

Field :   Sağlık Bilimleri

Journal Type :   Ulusal

Metrics
Article : 1.277
Cite : 193
Details
Medeniyet Medical Journal