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21hydroxylasedeficiency 21ohd behavioraldisorder conduct criteria diagnosis endocrinology genetics peds psychiatry
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
• This is also ... Signs/Symptoms/Complications ... vomiting • Late (shock ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds #pediatrics
Conduct Disorder (CD): Pathogenesis and clinical findings - Must have >3 symptoms present in the past
Conduct Disorder (CD ... underdiagnosed in females, as ... sexual activity • Bullies ... BehavioralDisorder #Pathophysiology ... #signs #psychiatry
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