3 results
signs 21hydroxylasedeficiency 21ohd behavioraldisorder conduct criteria endocrinology genetics otitismedia psychiatry
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... deficiencies present in infants ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children) Upper Respiratory Tract Infection: - Bacterial: Streptococcus
Pathogenesis and Clinical ... #OtitisMedia #pathophysiology ... #diagnosis #symptoms ... #signs #peds #pediatrics
Conduct Disorder (CD): Pathogenesis and clinical findings - Must have >3 symptoms present in the past
Pathogenesis and clinical ... present in the past 12 ... BehavioralDisorder #Pathophysiology ... #diagnosis #symptoms ... #signs #psychiatry
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