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differential metabolic syndrome algorithm alkalosis aniongap causes hypokalemia management nongap urinary urine
Gitelman Syndrome Pathophysiology Gitelman Syndrome is a rare autosomal recessive salt-losing tubulopathy with a prevalence of 1-
Pathophysiology ... thiazide-sensitive sodium-chloride ... delivery to distal nephron ... #Syndrome #Pathophysiology ... #nephrology #diagnosis
Metabolic Alkalosis - Urinary Chloride Algorithm Cl- responsive metabolic alkalosis • Kidney loss of Cl-
Bartter syndrome, Gitelman ... effect Normal gap ... In a normal gap ... urine #Algorithm #nephrology ... #differential #diagnosis
Causes of High-anion Gap and Non-anion Gap Metabolic Acidosis Causes of High-anion Gap Acidosis: • Lactic acidosis
of High-anion Gap ... Generalized distal nephron ... loads (ammonium chloride ... #differential #diagnosis ... #causes #nephrology
Gitelman Syndrome Overview What? • Inherited (AR) hypokalemic salt-losing tubulopathies affecting the thiazide-sensitive sodium chloride cotransporter • Gitelman's syndrome
Renal tubular acidosis ... • Congenital chloride ... #Syndrome #diagnosis ... #nephrology #management ... #pathophysiology
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