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PMID: 9378602 Published · ppublish English Journal Article Review

Inherited cerebellar diseases.

International review of neurobiology ·Vol. 41 ·1997-00-00 ·Pages 441-53

Wallesch CW, Bartels C

Abstract

This chapter analyzes the neuropsychological deficits in inherited cerebellar diseases and compares their symptomatology with animal models in which the exact anatomical localization of degeneration is known and limited to the cerebellum. Both animal and human data suggest that cerebellar cortical atrophy affects functions of the frontal lobe system. Olivopontocerebellar atrophy is genetically and clinically in homogeneous. The dementia syndrome that occurs in a proportion of patients does not seem to be linked with cerebellar dysfunction. Patients suffering from Friedreich's disease have been described as exhibiting cognitive slowing and deficits in spatial tasks. Because other structures are more prominently involved than the cerebellum in this disease, other pathoanatomical correlates may explain the symptomatology.

MeSH Terms
Animals Atrophy/genetics Cerebellar Diseases/genetics,pathology Cerebellum/pathology Disease Models, Animal Humans Myoclonus/genetics Neuropsychological Tests Olivopontocerebellar Atrophies/genetics
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Wallesch C W
Department of Neurology, Otto-von-Guericke University, Magdeburg, Germany.
Bartels C
Article Info
Journal
International review of neurobiology
Abbr.
Int Rev Neurobiol
ISSN
0074-7742
Published
1997-00-00
Pages
441-53
Language
English
Region
United States
NLM ID
0374740
Subset
IM
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