A concise review discussing the genetic abnormalities that lead to Gitelman Syndrome. Attention is also paid to the clinical features, differentiation from Bartter Syndrome, and common supportive measures.




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Estimated Time: 15 minutes
Target Audience: Fellows, Residents, Physician-Extenders
Title: Gitelman Syndrome
Citation: Orphanet Journal of Rare Diseases 2008, Volume 3, pp. 1-6
Date Created: 2008
Revisions: None Indicated
Disclaimers: None Indicated
Resource Type: Text
Recommend to a Colleague/Friend
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