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management 21hydroxylasedeficiency endocrinology etoh examination genetics newborn physicalexam sarcoidosis signs timeline treatment 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 •
Syndrome (AWS) ... Withdrawal Symptom ... Hallucinosis (12 ... with normal vital signs ... #AWS #diagnosis
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
is also a late sign ... When the diagnosis ... are observed for signs ... #Examination #Peds ... #Pediatrics #Diagnosis
Sarcoidosis - Diagnosis and Management Summary Epidemiology 1) High incidence in Scandinavian countries (11-24 cases per 100,000 individuals
Sarcoidosis - Diagnosis ... survival is 93-95% Pathophysiology ... mediators such as ... abnormal LFT): 12 ... #Management #Signs
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