4 results
ophthalmology symptoms ceap centralretinalartery classification complications crao disorders genetics hypertensive occlusion pediatrics praderwilli retinopathy syndrome veins venous
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... Syndrome Signs ... fractures • Short ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Chronic Hypertensive Retinopathy: Pathogenesis and clinical findings Ophthalmic Artery Hypertension Stage 1: Mild/vasoconstrictive • Acute and chronic vasospasm
Pathogenesis and clinical ... -> Cotton-wool Spots ... #Retinopathy #pathophysiology ... ophthalmology #diagnosis ... #signs #symptoms
Central Retinal Artery Occlusion: Pathogenesis and clinical findings • Inflammatory Disease: (i.e. GCA, SLE, GPA) ->
Pathogenesis and clinical ... -> Cherry-red spot ... perfusion of retinal arterioles ... ophthalmology #diagnosis ... #signs #symptoms
CEAP Classification of Chronic Venous Disorders Clinical: C0 - NO clinical signs C1 - Small
Classification of Chronic ... signs C1 - Small ... to prior DVT) Anatomy ... Perforating veins Pathophysiology ... Disorders #veins #diagnosis
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