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centralretinalartery diagnosis genetics occlusion pediatrics signs symptoms syndrome
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome ... fractures • Short ... pulmonale #PraderWilli ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Central Retinal Artery Occlusion: Pathogenesis and clinical findings • Inflammatory Disease: (i.e. GCA, SLE, GPA) ->
-> Cherry-red spot ... perfusion of retinal arterioles ... due to upstream CRAO ... #pathophysiology ... #ophthalmology
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