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21hydroxylasedeficiency diagnosis endocrinology genetics pediatrics preop preoperative risk stratification
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... endocrinology #peds
Preoperative Risk Evaluation Major Pre-Op Questions: 1. Does the patient have any modifiable risk factors that could be
Evaluation Major ... adverse events or complications ... Change in clinical ... Intraabdominal - Orthopedic ... #Risk #Evaluation
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