Bartter and Gitelman's Syndromes Report

Bartter and Gitelman's Syndromes Bartter and Gitelman's Syndromes are a spectrum of inherited tubulopathies sometimes difficult to distinguish, given the sharing of some characteristic metabolic abnormalities. These syndromes consist of impaired management of sodium, potassium and chloride in the renal tubules. Underlying genetic abnormalities impair the kidney's ability to reabsorb electrolytes, leading to typical signs and symptoms of the condition. 15 genes analyzed It is recommended if: This report is ideal for patients with a clinical suspicion of Bartter and Gitelman Syndromes. List of main conditions: Bartter syndrome, type 3 Bartter syndrome, type 5, antenatal, transient Bartter syndrome, type 1