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Search Results for FIP1L1-PDGFRA mutation
Abstract Number: 39
RARE CASE OF PRIMARY HYPEREOSINOPHILIC SYNDROME
SHM Converge 2024
Case Presentation: A 38-year-old Caucasian male with no significant prior medical history presented with an acute CVA based on the presence of fatigue, blurry vision, ataxia, headache, and numbness. His MRI showed “multiple small foci of high DWI/ADC signal” in the bilateral cerebral and cerebellar hemispheres consistent with small acute infarcts. Unremarkable CTA brain/neck, ECHO, [...]
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