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diabetes management pharmacology 21hydroxylasedeficiency 21ohd acromegaly agonists comparison diabetic diagnosis dka dpp4 genetics glp1 hhs hyperglycemic hyperosmolar inhibitors ketoacidosis pediatrics
Pathophysiology of Diabetic Ketoacidosis (DKA) and Hyperglycemic Hyperosmolar Syndrome (HHS) Absolute Insulin deficit: - Type I DM:
Pathophysiology ... deficit: - Type I DM ... food binges, etc Hyperglycemia ... #dka #hhs #pathophysiology ... #comparison #endocrinology
DPP4 Inhibitors - Normal and Renal Dosing Increase Incretins (GLP-I & GIP) -> Stimulates Insulin, Inhibits Glucagon
Normal and Renal Dosing ... minimal chance of hypoglycemia ... Inhibitors #Renal #Dosing ... Management #Diabetes #DM2 ... #Endocrinology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
mutation in CYP21A2 coding ... Hyperkalemia, Hypoglycemia ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
GLP-1 Agonists Adlyxin (Lixisenatide) Daily Bydureon (Exenatide ER) Weekly Ozempic (Semaglutide) Weekly Trulicity (Dulaglutide) Weekly Victoza (Liraglutide) Daily
a low risk of hypoglycemia ... #Pharmacology #Dosing ... #Diabetes #DM2 ... #Endocrinology
Acromegaly - Diagnosis and Management Summary - GrepMed Handbook Clinical Presentation: • Classic Acromegaly: frontal
Acromegaly: frontal bossing ... malignancy Pathophysiology ... Pegvisomant) ± D2 ... Diagnosis #Management #Endocrinology ... #Treatment #Pathophysiology
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