Literature DB >> 601115

[EEG studies of spinocerebellar ataxia].

G Sack, B Gruss, J Lössner, H Bachmann.   

Abstract

Electroencephalographic examinations of eighteen patients with spinocerebellar ataxias and of thirteen normal sibs of four of the subjects are reported. The authors frequently observed low levels of potential and a tendency toward slackening in basic activity, which is in agreement with data presented in the literature; theta-delta inclusions in the temporal regions were found especially in cases of cerebellar ataxia. Examinations of the sib frequently showed low-potential curves. However, the use of electroencephalography for the purpose of identifying, in the case of hereditary ataxia, latently diseased sibs for heterozygous individuals does not seem possible.

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Year:  1977        PMID: 601115

Source DB:  PubMed          Journal:  Psychiatr Neurol Med Psychol (Leipz)        ISSN: 0033-2739


  1 in total

1.  Hereditary cerebellar atrophy (Holmes type) with optic atrophy: a clinico-pathological study of four generations in a family.

Authors:  H Budka; D Seemann; W Danielczyk
Journal:  Arch Psychiatr Nervenkr (1970)       Date:  1979-04-12
  1 in total

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