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21hydroxylasedeficiency aws endocrinology etoh genetics management syndrome timeline withdrawal
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
deficiencies present in infants ... Signs/Symptoms/Complications ... #pathophysiology ... endocrinology #peds ... #pediatrics
Alcohol Withdrawal Syndrome (AWS) - ICU OnePager Scoring Alcohol Withdrawal Syndrome (AWS): • PAWSS • CIWA-Ar •
Withdrawal Symptom ... Minor Withdrawal Symptoms ... Hallucinosis (12 ... with normal vital signs ... Syndrome #AWS #diagnosis
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