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21hydroxylasedeficiency 21ohd bulimianervosa diagnosis endocrinology genetics pediatrics psychiatry 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 ... vomiting • Late (shock ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds
Bulimia Nervosa: Complications GASTROINTESTINAL • Dehydration & inability to digest food -> Constipation • Recurrent vomiting exposes
GASTROINTESTINAL • Dehydration ... frequent vomiting -> decreased ... hormone levels cause ... #pathophysiology ... #diagnosis #signs
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