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diagnosis nephrology management defects epithelial gitelman hyperkalemia kidney metabolic nagma nonaniongap normal pathophysiology potassium syndrome treatment tubule
Inherited Defects in Kidney Tubule Epithelial Cells Renal glucosuria - Na+-dependent glucose cotransporter Cystinuria - Amino acid transporter Bartter
Inherited Defects ... syndrome - Na-K- ... acidosis - alpha-Intercalated ... #Diagnosis #Differential ... #Table
Normal Anion-Gap Acidosis (NAGMA) - Differential Diagnosis Framework and Workup NAGMA - Chem, ABG or VBG - Calculate Anion
(NAGMA) - Differential ... Framework and Workup ... Hypoaldosteronism - Renal Tubular ... #Diagnosis #Workup ... #nephrology
Hyperkalemia - Diagnosis and Management - GrepMed Handbook S/Sx: Most pts asymptomatic. Weakness, cramping, nausea, paresthesias, palpitations,
reabsorption) Workup ... Elimination (see Table ... ) • Low K diet ... Slow - don’t delay ... Treatment #potassium #nephrology
Gitelman Syndrome Overview What? • Inherited (AR) hypokalemic salt-losing tubulopathies affecting the thiazide-sensitive sodium chloride cotransporter • Gitelman's syndrome
• Inherited (AR) ... distal convoluted tubule ... alkalosis • Normal or low ... ratio 0.5%) Differential ... acidosis (RTA))
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