|
|
|
Click Here to return To Results
|
|
Subacute sclerosing panencephalitis (SSPE) is mainly thought of as a disorder of childhood and adolesence and may not be readily recognized when presenting later in life. Prior reports have suggested that adult-onset SSPE may have atypical features. We have added two cases to the existing literature on adult-onset SSPE, compared them with a more classic juvenile presentsatation, and extensively reviewed those reports that were published after the etiological link with the measles virus has been established. The importance of recognizing the spectrum of potential presentations of SSPE and providing an early diagnosis will increase as more efffective treatments become available. |
|
(click to filter results - removes previous filter)
akinetic mute antibodies to measles atypical basal ganglia,lesion of brain biopsy brainstem,lesion of cerebellar lesion cerebellar peduncle cerebrospinal fluid,oligoclonal IgG in deep gray nuclei dementia electroencephalogram,periodic complexes heralding manifestation incidence intellectual deterioration mental status,abnormal middle cerebellar peduncle,lesion movement disorder myoclonus neuropathology reading disorder,acquired review article rubeola virus serologic testing subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease subacute sclerosing panencephalitis,adult onset thalamus,lesion of treatment of neurologic disorder viral infection,CNS visual loss visuospatial disturbance
|
Click Here to return To Results
|
|