4 results
diagnosis ophthalmology pediatrics symptoms anatomy centralretinalartery chronic complications crao fetal genetics hypertensive praderwilli retinopathy syndrome
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome ... 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
Hard Exudates • Occlusion ... -> 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) ->
Retinal Artery Occlusion ... -> Cherry-red spot ... perfusion of retinal arterioles ... #CRAO #pathophysiology ... ophthalmology #diagnosis #signs
Fetal and Post Transition Circulation In the fetal circulatory system, oxygenated blood is delivered via the umbilical
Post Transition Circulation ... through the ductus arteriosus ... #Pathophysiology ... #Cardiology #Anatomy ... #Peds #Pediatrics
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