Öztürk M.Si?irci A.Yakinci C.2024-08-042024-08-0420151757-790Xhttps://doi.org/10.1136/bcr-2015-209310https://hdl.handle.net/11616/91801Subacute sclerosing panencephalitis (SSPE) is a rare, slowly progressive, fatal, inflammatory and neurodegenerative disease that is seen mostly in children and young adolescents, and primarily affects the parieto-occipital lobes. The corpus callosum, cerebellum and basal ganglia are less frequently involved. MR spectroscopy (MRS) may illustrate the pathophysiological features of SSPE. To the best of our knowledge, this is the second report of MRS findings of corpus callosum involvement in a stage 3 SSPE case. Copyright 2015 BMJ Publishing Group. All rights reserved.eninfo:eu-repo/semantics/openAccessetiracetamlamotriginemethisoprinolmidazolamvalproic acidadd on therapyadolescentArticleatonic seizureBabinski reflexbrain atrophycase reportcerebrospinal fluidconsciousness disordercorpus callosumelectroencephalogramfollow upgeneralized epilepsyhospital dischargehospitalizationhumanmalemeaslesmyoclonus seizurenuclear magnetic resonance imagingnuclear magnetic resonance spectroscopypriority journalsubacute sclerosing panencephalitistendon reflexcorpus callosumpathophysiologysubacute sclerosing panencephalitisAdolescentCorpus CallosumHumansMagnetic Resonance ImagingMagnetic Resonance SpectroscopyMaleSubacute Sclerosing PanencephalitisArticle20152616355210.1136/bcr-2015-2093102-s2.0-84938945157Q3