2 results
21hydroxylasedeficiency behavioraldisorder conduct criteria endocrinology genetics signs
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
Conduct Disorder (CD): Pathogenesis and clinical findings - Must have >3 symptoms present in the past
Conduct Disorder (CD ... present in the past 12 ... BehavioralDisorder #Pathophysiology ... #diagnosis #symptoms ... #signs #psychiatry
No results found for "b12 peds video sign diagnosis infant pathophysiology symptoms pediatrics psychiatry 21ohd cd"
Try removing search terms or sorting by relevance
Or Upload an image for you and others searching for #b12 #peds #video #sign #diagnosis #infant #pathophysiology #symptoms #pediatrics #psychiatry #21ohd #cd