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diagnosis 21hydroxylasedeficiency cop differential genetics myelitis neurology organizing pediatrics pneumonia pulmonary transverse
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Cryptogenic Organizing Pneumonia - Illness Script PATHOPHYSIOLOGY: Unknown trigger, reversible inflammatory/fibroproliferative process. Polypoid fibroblastic aggregates that plug
Cryptogenic Organizing ... Illness Script PATHOPHYSIOLOGY ... Males=Females SIGNS ... identified (autoimmune, meds ... Pneumonia #diagnosis #management
Transverse Myelitis Overview Focal inflammatory disorder of the spinal cord resulting in rapid onset of weakness, sensory
monophasic Pathophysiology ... • Bilateral signs ... Herpes simplex virus ... Myelitis #diagnosis #management ... #neurology #differential
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