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diagnosis pathophysiology diabetic hhs hyperglycemic ketoacidosis pediatrics 21hydroxylasedeficiency 21ohd algorithm cah causes congenitaladrenalhyperplasia diabetes differential disorders genetics ketones ketosis laboratory
Ketosis Disorders - Comparison Table • Starvation Ketosis • Alcoholic Ketoacidosis (AKA) • Diabetic Ketoacidosis (DKA)
Ketosis Disorders - Comparison ... Ketoacidosis (DKA ... Hyperglycemic Hyperosmolar ... diagnosis #management #endocrinology ... #comparison #table
Pathophysiology of Diabetic Ketoacidosis (DKA) and Hyperglycemic Hyperosmolar Syndrome (HHS) Absolute Insulin deficit: - Type I DM:
Ketoacidosis (DKA ... Hyperglycemic Hyperosmolar ... food binges, etc Hyperglycemia ... pathophysiology #comparison ... #endocrinology
DKA vs HHS - Think of DKA and HHS on a spectrum of hyperglycemic emergencies -
of DKA and HHS ... #HHS #comparison ... laboratory #diagnosis #endocrinology ... #comparison #diabetic ... #ketoacidosis #hyperosmolar
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
of congenital adrenal ... CongenitalAdrenalHyperplasia #diagnosis #comparison ... #treatment #Peds ... #Endocrinology ... #Adrenal #pathophysiology
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 ... as "congenital adrenal ... Hyperkalemia, Hypoglycemia ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
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