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