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diagnosis pathophysiology 21hydroxylasedeficiency bulimianervosa endocrinology evaluation genetics pediatrics perioperative preop preoperative psychiatry risk stratification symptoms
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD ... endocrinology #peds
Preoperative Risk Evaluation Major Pre-Op Questions: 1. Does the patient have any modifiable risk factors that could be
adverse events or complications ... event, follow ACC algorithm ... Cataract Plan for Meds ... are needed: • HgbA1c ... or death (CARP, DECREASE
Bulimia Nervosa: Complications GASTROINTESTINAL • Dehydration & inability to digest food -> Constipation • Recurrent vomiting exposes
Bulimia Nervosa: Complications ... GASTROINTESTINAL • Dehydration ... frequent vomiting -> decreased ... hormone levels cause ... pathophysiology #diagnosis #signs
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