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21hydroxylasedeficiency diagnosis differential endocrinology genetics management myelitis pediatrics peds transverse
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 ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... endocrinology #peds #pediatrics
Transverse Myelitis Overview Focal inflammatory disorder of the spinal cord resulting in rapid onset of weakness, sensory
alterations, and bowel ... monophasic Pathophysiology ... • Bilateral signs ... • Infectious causes ... diagnosis #management #neurology
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