| Literature DB >> 11488899 |
E Trinka1, C Rauscher, M Nagler, T Moroder, G Ladurner, E Irnberger, W Sperl, P Pilz.
Abstract
We report a patient with early infantile epileptic encephalopathy (EIEE) with suppression-burst (Ohtahara syndrome) associated with olivary-dentate dysplasia and agenesis of mamillary bodies is reported. Although those with Ohtahara syndrome are a heterogeneous group, virtually all reported cases are secondary to neuronal migrational disorders, sometimes only identified by detailed neuropathologic examination, as in this case report, which describes mamillary body agenesis as a not-yet-recognized anomaly associated with Ohtahara syndrome. All children with Ohtahara syndrome should have high-resolution magnetic resonance imaging (MRI) and detailed postmortem neuropathologic examinations.Entities:
Mesh:
Year: 2001 PMID: 11488899 DOI: 10.1046/j.1528-1157.2001.042007950.x
Source DB: PubMed Journal: Epilepsia ISSN: 0013-9580 Impact factor: 5.864