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diagnosis pediatrics 21hydroxylasedeficiency disease endocrinology genetics incomplete kawasaki perioperative preop preoperative risk stratification
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 ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... endocrinology #peds
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
Evaluation of suspected ... Infants ≤6 months ... lack of tapering, decreased ... clinical and lab signs ... #Diagnosis #Peds
Preoperative Risk Evaluation Major Pre-Op Questions: 1. Does the patient have any modifiable risk factors that could be
Preoperative Risk Evaluation ... event, follow ACC algorithm ... are needed: • HgbA1c ... or death (CARP, DECREASE ... perioperative #Risk #Evaluation
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