2010
DOI: 10.1016/j.jocn.2009.12.016
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A 22-year-old Australian woman with atypical subacute sclerosing panencephalitis diagnosed at postmortem

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Cited by 9 publications
(9 citation statements)
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“…Another unusual feature of this patient was the rapid clinical course. About 10% of patients with SSPE follow an acute course, and acute cases are known to diverge from the classical clinical stages, and may lack both myoclonus and periodic EEG abnormalities, [12][13][14] similar to the present patient. Other atypical clinical presentations of SSPE include seizures and focal neurological deficits.…”
mentioning
confidence: 76%
“…Another unusual feature of this patient was the rapid clinical course. About 10% of patients with SSPE follow an acute course, and acute cases are known to diverge from the classical clinical stages, and may lack both myoclonus and periodic EEG abnormalities, [12][13][14] similar to the present patient. Other atypical clinical presentations of SSPE include seizures and focal neurological deficits.…”
mentioning
confidence: 76%
“…Generalized rigidity with extra-pyramidal features and unresponsiveness appear in stage 3. Stage 4 is the terminal stage of the disease and is characterized by minimal conscious state and later akinetic mutism associated with persistent high fevers and bouts of generalized sweating; both being due to autonomic failure3.The prognosis of SSPE is poor with death typically occurring within two to four years of onset as no curative treatment is available 3 . The diagnosis of SSPE is based on typical clinical features, periodic EEG complexes and elevated measles antibody titre in CSF.…”
Section: Discussionmentioning
confidence: 99%
“…SSPE remains an important public health issue in parts of the developing world due to limited measles immunization policies. 4 , 5 …”
Section: Discussionmentioning
confidence: 99%