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algorithm diagnosis hyperuricemia peds 21hydroxylasedeficiency 21ohd adrenal cah complications congenitaladrenalhyperplasia diabetes diabeticketoacidosis differential dka genetics treatment uricacid
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
CAH #algorithm #causes ... #pediatrics #CongenitalAdrenalHyperplasia ... #diagnosis #comparison ... treatment #Peds #Endocrinology ... #Adrenal #pathophysiology
Hyperuricemia - Differential Diagnosis Algorithm Primary - Over-production • Increased turnover of nucleotides Primary
Drug-induced • High purine ... • Alcohol #gout ... Diagnosis #Algorithm #endocrinology ... #causes
Diabetic Ketoacidosis (DKA) - Pathogenesis and Clinical Findings • Note: in DKA, body K+ is lost
diffusion of K+ out ... of cells may cause ... renal function/urine ... DiabeticKetoacidosis #DKA #pathophysiology ... #endocrinology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... non-arousable, decr urine ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Hyperuricemia: Pathogenesis and Complications - Hypercalcemia (due to diseases like Sarcoidosis and Hyperparathyroidism) -> Accumulation of
-> Release of purine ... bases -> Over-production ... Hyperuricemia #Pathophysiology ... Complications #Gout
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