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behavioraldisorder signs 21hydroxylasedeficiency adhd attentiondeficithyperactivedisorder cd conduct endocrinology genetics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
deficiencies present in infants ... Signs/Symptoms/Complications ... #pathophysiology ... endocrinology #peds ... #pediatrics
Attention Deficit Hyperactive Disorder (ADHD): Pathogenesis and clinical findings - For diagnosis, must have either 26
findings - For diagnosis ... BehavioralDisorder #Pathophysiology ... #diagnosis #symptoms ... #signs #psychiatry ... #criteria
Conduct Disorder (CD): Pathogenesis and clinical findings - Must have >3 symptoms present in the past
present in the past 12 ... BehavioralDisorder #Pathophysiology ... #diagnosis #symptoms ... #signs #psychiatry ... #criteria
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