Hereditary ataxias

Virgilio Gerald H. Evidente, Katrina A. Gwinn-Hardy, John N. Caviness, Sid Oilman

Research output: Contribution to journalReview article

62 Scopus citations

Abstract

There are many causes of hereditary ataxia. These can be grouped into categories of autosomal recessive, autosomal dominant, and X-linked. Molecularly, many of them are due to trinucleotide repeat expansions. In Friedreich ataxia, the trinucleotide repeat expansions lead to a 'loss of function.' In the dominant ataxias, the expanded repeats lead to a 'gain of function,' most likely through accumulation of intranuclear (and less commonly cytoplasmic) polyglutamine inclusions. Channelopathies can also lead to ataxia, especially episodic ataxia. Although phenotypic characteristics are an aid to the clinician, a definitive diagnosis is usually made only through genotypic or molecular studies. Genetic counseling is necessary for the testing of symptomatic and asymptomatic individuals. No effective treatment is yet available for most ataxic syndromes, except for ataxia with isolated vitamin E deficiency and the episodic ataxias.

Original languageEnglish (US)
Pages (from-to)475-490
Number of pages16
JournalMayo Clinic proceedings
Volume75
Issue number5
DOIs
StatePublished - 2000

ASJC Scopus subject areas

  • Medicine(all)

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    Evidente, V. G. H., Gwinn-Hardy, K. A., Caviness, J. N., & Oilman, S. (2000). Hereditary ataxias. Mayo Clinic proceedings, 75(5), 475-490. https://doi.org/10.4065/75.5.475