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pathophysiology diagnosis ophthalmology 21hydroxylasedeficiency centralretinalartery chronic complications crao endocrinology genetics hypertensive occlusion pediatrics peds retinopathy
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Females may be labeled ... Signs/Symptoms/Complications ... enlarged penis months after ... #21HydroxylaseDeficiency #21OHD
Central Retinal Artery Occlusion: Pathogenesis and clinical findings • Inflammatory Disease: (i.e. GCA, SLE, GPA) ->
trucking" • Acute ... retinal edema caused ... CRAO -> Pale Optic ... ophthalmology #diagnosis #signs ... #symptoms
Chronic Hypertensive Retinopathy: Pathogenesis and clinical findings Ophthalmic Artery Hypertension Stage 1: Mild/vasoconstrictive • Acute and chronic vasospasm
Ophthalmic Artery ... vasoconstrictive • Acute ... Leakage of optic ... ophthalmology #diagnosis #signs ... #symptoms #complications
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