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Gitelman syndrome associated with chondrocalcinosis: description of two cases

Gitelman syndrome is a rare inherited tubulopathy, characterized by hypomagnesemia, hypokalemia, metabolic alkalosis, hypocalciuria and hyperreninemic hyperaldosteronism. The clinical spectrum is wide and includes: cramps, myalgies, muscle weakness, until episodes of carpo-podalic spasm, tetania, ra...

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Autors principals: E. Filippucci, L. Di Geso, M. Tardella, G. Giacchetti, C. Bertolazzi, F. Silveri, M. Gutierrez, W. Grassi
Format: Artigo
Idioma:Inglês
Publicat: PAGEPress Publications 2011-06-01
Col·lecció:Reumatismo
Accés en línia:http://www.reumatismo.org/index.php/reuma/article/view/464
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