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21hydroxylasedeficiency behavioraldisorder cd conduct criteria cystitis emphysematous endocrinology genetics management peds signs
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Signs/Symptoms/Complications ... non-arousable, decr urine ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology
Emphysematous Cystitis Epidemiology: • Usually middle-aged diabetic women • Other RF: neurogenic bladder, urinary tract outlet obstruction,
immune compromise Clinical ... Signs/Symptoms: ... Pathophysiology: ... KUB or abdominal ultrasound ... present • UA and Urine
Conduct Disorder (CD): Pathogenesis and clinical findings - Must have >3 symptoms present in the past
Pathogenesis and clinical ... - Must have >3 symptoms ... BehavioralDisorder #Pathophysiology ... #diagnosis #symptoms ... #signs #psychiatry
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