3 results
diagnosis symptoms 21hydroxylasedeficiency centralretinalartery chronic complications crao endocrinology genetics hypertensive occlusion pediatrics retinopathy
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... enzyme 21-OHase causes ... Signs/Symptoms/Complications ... #pathophysiology ... endocrinology #peds
Chronic Hypertensive Retinopathy: Pathogenesis and clinical findings Ophthalmic Artery Hypertension Stage 1: Mild/vasoconstrictive • Acute and chronic vasospasm
Pathogenesis and clinical ... fluffy white ischemic ... #Retinopathy #pathophysiology ... #ophthalmology ... #diagnosis #signs
Central Retinal Artery Occlusion: Pathogenesis and clinical findings • Inflammatory Disease: (i.e. GCA, SLE, GPA) ->
Pathogenesis and clinical ... retinal edema caused ... Occlusion #CRAO #pathophysiology ... #ophthalmology ... #diagnosis #signs
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