The Calgary Guide to Understanding Disease @TheCalgaryGuide
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21hydroxylasedeficiency conduct criteria 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
Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... endocrinology #peds
Conduct Disorder (CD): Pathogenesis and clinical findings - Must have >3 symptoms present in the past
Conduct Disorder (CD ... However, CD may ... #BehavioralDisorder ... #Pathophysiology ... diagnosis #symptoms #signs
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