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diagnosis 21hydroxylasedeficiency 21ohd bulimianervosa complications endocrinology genetics management pheochromocytoma psychiatry treatment
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 #pathophysiology ... endocrinology #peds ... #pediatrics
Pheochromocytoma - Diagnosis and Management Summary 10 percent rule = 10% of pheochromocytomas are extra-adrenal, multiple, bilateral,
bilateral, malignant, pediatric ... cases, not associated ... and Signs: 50% ... and signs: • ... polyuria, polydipsia, constipation
Bulimia Nervosa: Complications GASTROINTESTINAL • Dehydration & inability to digest food -> Constipation • Recurrent vomiting exposes
digest food -> Constipation ... frequent vomiting -> decreased ... hormone levels cause ... #diagnosis #signs ... #symptoms #psychiatry
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