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diagnosis centralretinalartery disease genetics incomplete kawasaki occlusion praderwilli signs symptoms syndrome
Central Retinal Artery Occlusion: Pathogenesis and clinical findings • Inflammatory Disease: (i.e. GCA, SLE, GPA) ->
Pathogenesis and clinical ... -> Cherry-red spot ... #pathophysiology ... #ophthalmology ... #diagnosis #signs
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... Prader-Willi Syndrome Signs ... fractures • Short ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
if they have no clinical ... effusion, or z scores ... and lab signs ( ... #Diagnosis #Peds ... #Pediatrics #Kawasaki
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