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diabetes pediatrics comparison 21hydroxylasedeficiency 21ohd algorithm assessment cah causes congenitaladrenalhyperplasia diabetic diagnosis dka dm1 dosing dpp4 genetics hhs hyperglycemic hyperosmolar
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
of congenital adrenal ... comparison #treatment #Peds ... #Endocrinology ... #Adrenal #pathophysiology
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
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
21-OHD in the adrenal ... Hyperkalemia, Hypoglycemia ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
DPP4 Inhibitors - Normal and Renal Dosing Increase Incretins (GLP-I & GIP) -> Stimulates Insulin, Inhibits Glucagon
Inhibitors - Normal and Renal ... minimal chance of hypoglycemia ... patients have renal ... Management #Diabetes #DM2 ... #Endocrinology
Assessment of diabetic control: - Any episodes of hypoglycaemia, diabetic ketoacidosis, hospital admission? - Is
Any episodes of hypoglycaemia ... still awareness of hypoglycaemia ... centiles) - Renal ... #primarycare #DM1 ... #Peds #Pediatrics
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