Asymptomatic spinal cord involvement in posterior reversible encephalopathy syndrome.
Neurology (Impact Factor: 8.3). 05/2010; 74(18):1478-9; author reply 1479. DOI: 10.1212/WNL.0b013e3181d8a4a3
Article: [Demyelinating disorders].[Show abstract] [Hide abstract]
ABSTRACT: Leukoencephalopathies in adults are frequent and exhibit highly variable aetiology, including multiple acquired causes such as inflammatory, vascular or toxic diseases and neoplasias. In contrast leukodystrophies are genetically determined, chronic progressive myelin disorders with a variable pathogenetic background and a great diversity of clinical and paraclinical findings. Some diseases, namely those with an additional inborn error of metabolism, are treatable. Genetic counselling appears to be of major importance for patients and their families. In the light of numerous acquired adulthood leukoencephalopathies a clear delineation of late-onset genetic leukodystrophies is necessary. Clinical symptoms and MRI patterns of some of the major leukodystrophies are reported, including possibilities of biochemical and genetic testing.Der Nervenarzt 03/2010; 81(4):471-96. · 0.80 Impact Factor
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