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21hydroxylasedeficiency bulimianervosa complications diagnosis genetics pediatrics peds 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 ... urine output • Hirsutism ... & acne • Infertility ... #pathophysiology ... #genetics #endocrinology
Bulimia Nervosa: Complications GASTROINTESTINAL • Dehydration & inability to digest food -> Constipation • Recurrent vomiting exposes
• Boerhaave syndrome ... Calcium, VitD) and ... hormone levels cause ... Complications #pathophysiology ... #diagnosis #signs
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