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21hydroxylasedeficiency diabetes diagnosis differential dpp4 genetics inhibitors management pathophysiology pediatrics peds pharmacology renal weightloss
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
mutation in CYP21A2 coding ... enzyme 21-OHase causes ... #21HydroxylaseDeficiency #21OHD ... pathophysiology #genetics #endocrinology
DPP4 Inhibitors - Normal and Renal Dosing Increase Incretins (GLP-I & GIP) -> Stimulates Insulin, Inhibits Glucagon
Normal and Renal Dosing ... patients have renal insufficiency ... Inhibitors #Renal #Dosing ... Management #Diabetes #DM2 ... #Endocrinology
Weight Loss - Differential Diagnosis Algorithm Decreased Intake: • GI illness (upper and lower) • Psychiatric (Depression,
Differential Diagnosis Algorithm ... • Pancreatic Insufficiency ... Disease • Protein-losing ... Failure • Adrenal Insufficiency ... #Causes
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