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birth growthcharts height length percentiles 21hydroxylasedeficiency 21ohd behavioraldisorder boys cd criteria endocrinology females genetics girls males 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 ... decr feeding, weight ... endocrinology #peds ... #pediatrics
This chart shows the patterns of height (length) and weight for children from birth to 36
76 cm) tall and 12 ... Consult your physician ... #Diagnosis #Peds ... #Pediatrics #GrowthCharts ... Females #Birth #Infant
This chart shows the patterns of height (length) and weight for children from birth to 36
76 cm) tall and 12 ... Consult your physician ... #Diagnosis #Peds ... #Pediatrics #GrowthCharts ... #Males #Birth #Infant
Conduct Disorder (CD): Pathogenesis and clinical findings - Must have >3 symptoms present in the past
Conduct Disorder ... present in the past 12 ... BehavioralDisorder #Pathophysiology ... #diagnosis #symptoms ... #signs #psychiatry
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