Olivopontocerebellaris atrophia IV. típusának családi halmozódása.

Translated title of the contribution: Cumulative familial olivopontocerebellar atrophy type IV

E. Erös, E. Czeizel

Research output: Contribution to journalArticle

Abstract

Three affected members of a family with olivopontocerebellar atrophy IV (Schut-Haymaker type) of autosomal dominant inheritance are presented. The five types of olivopontocerebellar atrophy are differentiated on the basis of clinical symptoms and the mode of inheritance. Its clinical symptoms are varied but the cerebellar ataxia of different extent is present in every case which may be followed by pyramidal and extrapyramidal symptoms. Clear differentiation from the other types is based on the destruction of the nuclei of cranial cerebral nerves (IX, X, XII).

Translated title of the contributionCumulative familial olivopontocerebellar atrophy type IV
Original languageHungarian
Pages (from-to)801-804
Number of pages4
JournalOrvosi hetilap
Volume135
Issue number15
Publication statusPublished - Apr 10 1994

ASJC Scopus subject areas

  • Medicine(all)

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