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21hydroxylasedeficiency diagnosis differential endocrinology genetics hyponatremia pathophysiology pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
mutation in CYP21A2 coding ... enzyme 21-OHase causes ... wasting crisis & hyperkalemia ... #21HydroxylaseDeficiency #21OHD ... endocrinology #peds
Causes of Hyponatremia - Differential Diagnosis Algorithm Hypovolemia, UNa > 20: • Renal losses, Diuretic excess,
Causes of Hyponatremia ... Differential Diagnosis Algorithm ... deficiency, Salt-losing ... renal failure Hypervolemia ... #Causes #nephrology
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