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algorithm diagnosis pediatrics peds 21hydroxylasedeficiency 21ohd cah comparison complications congenitaladrenalhyperplasia diabetes diabeticketoacidosis differential genetics gout hyperuricemia hypophosphatemia lowphosphate treatment
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
of congenital adrenal ... CAH #algorithm #causes ... treatment #Peds #Endocrinology ... #Adrenal #pathophysiology
Diabetic Ketoacidosis (DKA) - Pathogenesis and Clinical Findings • Note: in DKA, body K+ is lost
Ketoacidosis (DKA ... out of cells may cause ... patient has good renal ... #pathophysiology ... #endocrinology
Hypophosphatemia - Differential Diagnosis Algorithm Transcellular Shift • Recovery From DKA • Refeeding Syndrome • Acute Respiratory
Recovery From DKA ... Increased Excretion - Renal ... Diagnosis #Algorithm #endocrinology ... #causes
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... 21-OHD in the adrenal ... as "congenital adrenal ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology
Hyperuricemia: Pathogenesis and Complications - Hypercalcemia (due to diseases like Sarcoidosis and Hyperparathyroidism) -> Accumulation of
of calcium in renal ... Incr Breakdown of DNA ... Release of purine bases ... Hyperuricemia #Pathophysiology
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