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21hydroxylasedeficiency 21ohd genetics hypercalcemia malignancy pathophysiology peds treatment
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Hypoglycemia • Early ... urine output • Hirsutism ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
Treatment algorithm for malignancy-associated hypercalcemia. Hypercalcemia - Renal Failure → Dialysis with low Ca++ bath Aggressive IV hydration
Treatment algorithm ... for malignancy-associated ... Hypercalcemia - Renal ... Calcitonin Refractory Cases ... #management #endocrinology
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