Neurophysiological findings in the hereditary presenile dementia characterised by polycystic lipomembranous osteodysplasia and sclerosing leukoencephalopathy

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Abstract

17 patients suffering from the presenile dementia characterised by polycystic lipomembranous osteodysplasia and sclerosing leukoencephalopathy were studied neurophysiologically. Noteworthy findings were diffuse slowing, the accentuation of 6-8 Hz parasagittal activity, slowing of the dominant occipital rhythm and, in the late phase when 13 of patients got epileptic seizures, there was paroxysmal activity in the EEG.

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Hakola, H. P. A., & Partanen, V. S. J. (1983). Neurophysiological findings in the hereditary presenile dementia characterised by polycystic lipomembranous osteodysplasia and sclerosing leukoencephalopathy. Journal of Neurology Neurosurgery and Psychiatry, 46(6), 515–520. https://doi.org/10.1136/jnnp.46.6.515

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