8 results
Renal Tubular Acidosis (RTA) Diagnosis and Management
 • Distal (type 1) RTA
 • Proximal (type 2)
Renal Tubular Acidosis ... (RTA) Diagnosis ... #rta #Renal #Tubular ... #Acidosis #Diagnosis ... #table
Renal Tubular Acidosis (RTA) 
Type 1 - Failure of secretion
Type 2 - Bicarbonate wasting
Type 4 -
Renal Tubular Acidosis ... Hypoaldosteronism Mixed* - Inherited ... salt diet #Renal ... #Tubular #Acidosis ... #nephrology #diagnosis
Inherited Defects in Kidney Tubule Epithelial Cells

Renal glucosuria - Na+-dependent glucose cotransporter
Cystinuria - Amino acid transporter
Bartter
Inherited Defects ... Epithelial Cells Renal ... tubular acidosis ... #Diagnosis #Differential ... #Table
Normal Anion-Gap Acidosis (NAGMA) - Differential Diagnosis Framework and Workup

NAGMA
- Chem, ABG or VBG
- Calculate Anion
Normal Anion-Gap Acidosis ... - Differential Diagnosis ... Tubular Acidosis ... #Differential #Diagnosis ... #Workup #nephrology
Causes of Non-Gap Metabolic Acidosis - Differential Diagnosis Algorithm
Normal Anion Gap (<14) (Loss of Bicarbonate) -
Non-Gap Metabolic Acidosis ... - Differential Diagnosis ... Diarrhea • Fistula Renal ... Cell Problem - Low ... MetabolicAcidosis #NonGap
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 ... tubular acidosis ... (RTA)) • Refeeding ... Gitelman #Syndrome #diagnosis
Metabolic Causes of Kidney Stones in Children
 • Calcium Oxalate: Primary Hyperoxaluria type 1-3, Secondary Hyperoxaluria
Tubular Acidosis ... (RTA), Bartter ... Syndrome type 1-4, Lowe ... (Oculo-Cerebro-Renal ... #differential #diagnosis
Hyperkalemia - Diagnosis and Management - GrepMed Handbook

S/Sx: Most pts asymptomatic. Weakness, cramping, nausea, paresthesias, palpitations,
Hyperkalemia - Diagnosis ... Renin/Aldosterone, RTA ... Elimination (see Table ... ) • Low K diet ... Treatment #potassium #nephrology