8 results
diagnosis peds causes differential management 21hydroxylasedeficiency 21ohd atrioventricular cah comparison congenitaladrenalhyperplasia cushion defect diabetes endocardial genetics hypocalcemia hypophosphatemia lowcalcium lowphosphate
Pediatric Diabetic Ketoacidosis #Management #Peds #DKA #DiabeticKetoacidosis #Algorithm #PEMSource
Pediatric Diabetic ... Management #Peds #DKA ... #DiabeticKetoacidosis ... #Algorithm #PEMSource
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
of congenital adrenal ... #CAH #algorithm ... #causes #pediatrics ... treatment #Peds #Endocrinology ... #Adrenal #pathophysiology
Diabetic Ketoacidosis (DKA) - Pathogenesis and Clinical Findings • Note: in DKA, body K+ is lost
Ketoacidosis (DKA ... patient has good renal ... confusion coma #DiabeticKetoacidosis ... #DKA #pathophysiology ... #endocrinology
Atrioventricular Septal Defect aka AV canal defect aka endocardial cushion defect • Epidemiology and Associations • Embryology
Septal Defect aka ... AV canal defect aka ... Physical Exam • Pathophysiology ... management #peds #pediatrics ... #cardiology
Hypophosphatemia - Differential Diagnosis Algorithm Transcellular Shift • Recovery From DKA • Refeeding Syndrome • Acute Respiratory
Differential Diagnosis Algorithm ... Recovery From DKA ... Increased Excretion - Renal ... Differential #Diagnosis #Algorithm ... #endocrinology
Short Stature - Differential Diagnosis Algorithm Normal Variant, Normal Puberty Onset (BA = CA) • Familial Short
Differential Diagnosis Algorithm ... • Congenital Adrenal ... Differential #Diagnosis #Algorithm ... #endocrinology ... #causes #pediatrics
Hypocalcemia - Differential Diagnosis Algorithm - Low and High PTH LOW PTH - Hypoparathyroid - Congenital (Pediatric)
Differential Diagnosis Algorithm ... - Congenital (Pediatric ... • Chronic Renal ... Differential #Diagnosis #Algorithm ... #PTH #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 ... as "congenital adrenal ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
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