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nephrology differential defects gitelman hypokalemia kidney management metabolic nonaniongap normal pathophysiology syndrome tubule workup
Inherited Defects in Kidney Tubule Epithelial Cells Renal glucosuria - Na+-dependent glucose cotransporter Cystinuria - Amino acid transporter Bartter
Inherited Defects ... tubular acidosis ... #Epithelial #Inherited ... #Diagnosis #Differential ... #Table
Normal Anion-Gap Acidosis (NAGMA) - Differential Diagnosis Framework and Workup NAGMA - Chem, ABG or VBG - Calculate Anion
Diagnosis Framework ... Tubular Acidosis ... normal Type 4: Hyperkalemic ... #Differential #Diagnosis ... #Workup #nephrology
Gitelman Syndrome Overview What? • Inherited (AR) hypokalemic salt-losing tubulopathies affecting the thiazide-sensitive sodium chloride cotransporter • Gitelman's syndrome
• Inherited (AR) ... alkalosis • Normal or low ... (renal potassium ... tubular acidosis ... Gitelman #Syndrome #diagnosis
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