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21hydroxylasedeficiency diagnosis endocrinology genetics neurology pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Signs/Symptoms/Complications ... non-arousable, decr urine ... #pathophysiology ... endocrinology #peds
The Neurological Evaluation of a Comatose Patient Definition: • Coma: a state of unresponsiveness; the absence of
• Mutism Pathophysiology ... • Vestibulo-ocular ... • Examine for signs ... Casey Albin MD @ ... caseyalbin #PhysicalExam
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