4 results
diagnosis signs ophthalmology centralretinalartery chronic complications crao genetics hypertensive pediatrics peds praderwilli retinopathy serotonin
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome ... Pathogenesis and clinical ... Signs/Symptoms ... fractures • Short ... #genetics #pathophysiology
Central Retinal Artery Occlusion: Pathogenesis and clinical findings • Inflammatory Disease: (i.e. GCA, SLE, GPA) ->
Pathogenesis and clinical ... -> Cherry-red spot ... #CRAO #pathophysiology ... ophthalmology #diagnosis #signs ... #symptoms
Chronic Hypertensive Retinopathy: Pathogenesis and clinical findings Ophthalmic Artery Hypertension Stage 1: Mild/vasoconstrictive • Acute and chronic vasospasm
Pathogenesis and clinical ... Hard Exudates • Occlusion ... #Retinopathy #pathophysiology ... ophthalmology #diagnosis #signs ... #symptoms #complications
Serotonin Syndrome: Pathogenesis and Clinical Findings Serotonin Syndrome: Variable combination of mental status changes, autonomic instability, and
Serotonin Syndrome ... Pathogenesis and Clinical ... #Pathophysiology ... #Psychiatry #Diagnosis ... #Signs #Symptoms
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