Abstract:
:A young man with normal neurodevelopment presented with 3 years of medically refractory, progressive epilepsy and myoclonus. Initial examination included neuroimaging, electroencephalography, and biochemical analyses, all of which were unremarkable except for mildly enlarged ventricles. Over the following year, the patient experienced rapid cognitive decline with new-onset recurrent visual hallucinations and progressive lethargy. Results of subsequent electroencephalography and brain imaging were unchanged, and a fluorodeoxyglucose F 18 positron emission tomographic scan was normal.
journal_name
JAMA Neuroljournal_title
JAMA neurologyauthors
Cohen AL,Jones LK,Parisi JE,Klaas JPdoi
10.1001/jamaneurol.2016.3195subject
Has Abstractpub_date
2017-06-01 00:00:00pages
737-740issue
6eissn
2168-6149issn
2168-6157pii
2614285journal_volume
74pub_type
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