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diagnosis anions ataxia causes clinical defects epithelial gait gap gitelman hypokalemia inherited kidney management metabolic neurology parkinsonism pathophysiology physicalexam syndrome
Unmeasured Anions Associated with an Elevated Anion Gap and Metabolic Acidosis #Unmeasured #Anions #Gap #Metabolic #Acidosis #Diagnosis
and Metabolic Acidosis ... Gap #Metabolic #Acidosis ... #Diagnosis #Nephrology ... #Table #Differential
Inherited Defects in Kidney Tubule Epithelial Cells Renal glucosuria - Na+-dependent glucose cotransporter Cystinuria - Amino acid transporter Bartter
renal tubular acidosis ... Defects #Kidney #Nephrology ... #Diagnosis #Differential ... #Table
Tandem Gait Ataxia in Atypical Parkinsonism How to differentiate Parkinson’s disease from atypical Parkinsonism in a jiffy?
Gait Ataxia in Atypical ... Parkinsonism How to differentiate ... s disease from atypical ... PD patients are able ... #physicalexam #neurology
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 Gitelman Syndrome Overview What? • Inherited (AR) hypokalemic salt-losing tubulopathies affecting the thiazide-sensitive sodium chloride cotransporter • Gitelman's syndrome
present in the apical ... ratio 0.5%) Differential ... Renal tubular acidosis ... Syndrome #diagnosis #nephrology
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