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Encephalopathy with astrocitic residual bodies. Report of a case and rewiev of the literature

dc.contributor.authorFigols, J.es
dc.contributor.authorCervós-Navarro, J.es
dc.contributor.authorWolman, M.
dc.date.accessioned2011-01-17T12:38:56Z
dc.date.available2011-01-17T12:38:56Z
dc.date.issued1986
dc.description.abstractBiopsy and autopsy findings in a girl who died at 7% months after having suffered from progressive axial hypotonia, myoclonus, EEG changes and retarded psychomotor development. Inclusions consisting of lamellar profiles, situated in membrane-bound cytosomes were found mainly in astrocytes, but also in neurones and in axons of peripheral nerves. Lipofuscin bodies were also increased in number. The patient belongs in the same category as cases studied by Towfighi et al. (1975) and Martin et al. (1977). Etiology and pathogenesis of this syndrome remain unknown. It is suggested, however, that the pathological changes observed might have been caused by the administration soon after birth of anti-epileptic dmgs (diphenylhydantoin, clonazepam and nitrazepan).
dc.formatapplication/pdfes
dc.format.extent9es
dc.identifier.issn0213-3911es
dc.identifier.urihttp://hdl.handle.net/10201/17801
dc.languageenges
dc.publisherMurcia : F. Hernándezes
dc.relation.ispartofHistology and histopathologyes
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.subjectProgressive axial hypotoniaes
dc.subjectMyoclonuses
dc.subject.otherCDU::6 - Ciencias aplicadas::61 - Medicina::616 - Patología. Medicina clínica. Oncología::616.8 - Neurología. Neuropatología. Sistema nerviosoes
dc.titleEncephalopathy with astrocitic residual bodies. Report of a case and rewiev of the literaturees
dc.typeinfo:eu-repo/semantics/articlees
dspace.entity.typePublicationes
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