4 results
diagnosis symptoms behcet centralretinalartery chronic complications crao disease genetics hypertensive management occlusion peds praderwilli retinopathy
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome ... Signs/Symptoms ... fractures • Short ... #genetics #pathophysiology ... #peds #pediatrics
Chronic Hypertensive Retinopathy: Pathogenesis and clinical findings Ophthalmic Artery Hypertension Stage 1: Mild/vasoconstrictive • Acute and chronic vasospasm
narrowing and vascular ... -> Cotton-wool Spots ... #Retinopathy #pathophysiology ... #ophthalmology ... #diagnosis #signs
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
Behçet's Syndrome ... and diplopia) • Vascular ... inhibitors • Uveitis- Ophthalmology ... diagnosis #management #signs ... #symptoms #rheumatology
Central Retinal Artery Occlusion: Pathogenesis and clinical findings • Inflammatory Disease: (i.e. GCA, SLE, GPA) ->
Valvular, arrhythmias ... -> Cherry-red spot ... Occlusion #CRAO #pathophysiology ... #ophthalmology ... #diagnosis #signs
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