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21hydroxylasedeficiency behavioraldisorder conduct criteria differential endocrinology genetics management myelitis neurology pediatrics psychiatry signs transverse
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 ... #pathophysiology ... endocrinology #peds
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
Transverse Myelitis Overview Focal inflammatory disorder of the spinal cord resulting in rapid onset of weakness, sensory
monophasic Pathophysiology ... Transverse Myelitis - Clinical ... • Bilateral signs ... and/or symptoms ... - Sjogren - Vasculitis
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