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diagnosis differential 21hydroxylasedeficiency causes genetics hypocalcemia lowcalcium pathophysiology peds pth shortstature
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
wasting crisis & hyperkalemia ... Labia major & minor ... #21HydroxylaseDeficiency #21OHD ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
Hypocalcemia - Differential Diagnosis Algorithm - Low and High PTH LOW PTH - Hypoparathyroid - Congenital (Pediatric)
Hypocalcemia - Differential ... Diagnosis Algorithm ... - Congenital (Pediatric ... laxatives) #Hypocalcemia ... #PTH #endocrinology
Short Stature - Differential Diagnosis Algorithm Normal Variant, Normal Puberty Onset (BA = CA) • Familial Short
Differential Diagnosis Algorithm ... Inborn Metabolism Error ... Differential #Diagnosis #Algorithm ... #endocrinology ... #causes #pediatrics
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