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21hydroxylasedeficiency 21ohd buprenorphine endocrinology genetics initiation inpatient management opiate pathophysiology prescribing start
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
occur in utero as ... Signs/Symptoms/Complications ... Labia major & minor ... endocrinology #peds ... #pediatrics
Quick Guide: Buprenorphine Initiation Algorithm Adjunctive meds: The following can be prescribed PRN for symptoms of withdrawal
Adjunctive meds ... prescribed PRN for symptoms ... hours PRN w/d symptoms ... from previous day as ... #Addiction #Opiate
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