3 results
diagnosis symptoms centralretinalartery chronic complications crao genetics hypertensive occlusion pediatrics retinopathy syndrome
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Syndrome Signs ... fractures • Short ... pulmonale #PraderWilli ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Chronic Hypertensive Retinopathy: Pathogenesis and clinical findings Ophthalmic Artery Hypertension Stage 1: Mild/vasoconstrictive • Acute and chronic vasospasm
-> Cotton-wool Spots ... -> Elschnig's Spots ... #Retinopathy #pathophysiology ... #ophthalmology ... #diagnosis #signs
Central Retinal Artery Occlusion: Pathogenesis and clinical findings • Inflammatory Disease: (i.e. GCA, SLE, GPA) ->
-> Cherry-red spot ... perfusion of retinal arterioles ... Occlusion #CRAO #pathophysiology ... #ophthalmology ... #diagnosis #signs
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