| Literature DB >> 11442164 |
R A Marrie1, E A Shoubridge, J P Antel, D L Arnold, J Chen, E Andermann, F Andermann.
Abstract
We describe a patient with progressive myoclonus epilepsy (PME), white matter hyperintensities in the corpus callosum, cerebral hemispheres, and left cerebral peduncle on magnetic resonance imaging (MRI), and positive oligoclonal bands. A phosphorus magnetic resonance spectrum was compatible with mitochondrial dysfunction. Abnormal white matter signals are not a feature of the known PME syndromes, although they occur in Leber's hereditary optic neuropathy (LHON). These abnormalities oriented the diagnosis toward mitochondrial disease.Entities:
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Year: 2001 PMID: 11442164 DOI: 10.1046/j.1528-1157.2001.15800.x
Source DB: PubMed Journal: Epilepsia ISSN: 0013-9580 Impact factor: 5.864