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21hydroxylasedeficiency differential endocrinology etoh evaluation falls genetics geriatrics management neurology pathophysiology recurrent 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
Evaluation of Recurrent Falls Core Concept: Maintaining an upright posture requires the integrated function of multiple systems. Disruption in
presyncope, exertional symptoms ... positive Romberg sign ... Examples: - Dementia ... Cerebellar stroke - Alcohol-related ... Recurrent #Falls #Diagnosis
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