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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.

************************************** 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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