Literature DB >> 18094871

Atypical subacute sclerosing panencephalitis: case report.

Marcelo Maroco Cruzeiro1, Thiago Cardoso Vale, Leopoldo Antônio Pires, Gláucio Mendes Franco.   

Abstract

Subacute sclerosing panencephalitis (SSPE) is a progressive inflammatory disorder of the central nervous system with both poor prognosis and high mortality. The disease has been related to a persistent and aberrant measles virus infection and no effective treatment has been available. We report a case of SSPE with atypical features including seizures at onset and a fulminant course in a 8 years-old boy who had been previously immunized against measles.

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Year:  2007        PMID: 18094871     DOI: 10.1590/s0004-282x2007000600024

Source DB:  PubMed          Journal:  Arq Neuropsiquiatr        ISSN: 0004-282X            Impact factor:   1.420


  2 in total

1.  Epilepsia partialis continua in children with fulminant subacute sclerosing panencephalitis.

Authors:  Ruzica Kravljanac; Nebojsa Jovic; Milena Djuric; Ljubica Nikolic
Journal:  Neurol Sci       Date:  2010-10-30       Impact factor: 3.307

2.  Subacute sclerosing panencephalitis in a child with recurrent febrile seizures.

Authors:  Ayşe Kartal; Ayşegül Neşe Çıtak Kurt; Tuğba Hirfanoğlu; Kürşad Aydın; Ayşe Serdaroğlu
Journal:  Case Rep Pediatr       Date:  2015-02-24
  2 in total

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