The Calgary Guide to Understanding Disease @TheCalgaryGuide
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21hydroxylasedeficiency crao diagnosis endocrinology genetics occlusion peds symptoms
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 ... endocrinology #peds #pediatrics
Central Retinal Artery Occlusion: Pathogenesis and clinical findings • Inflammatory Disease: (i.e. GCA, SLE, GPA) ->
Visual Acuity #CentralRetinalArtery ... Occlusion #CRAO #pathophysiology ... #ophthalmology ... #diagnosis #signs
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