A new autosomal dominant pure cerebellar ataxia

E. Storey, R. J.M. Gardner*, M. A. Knight, M. L. Kennerson, R. R. Tuck, S. M. Forrest, G. A. Nicholson

*Corresponding author for this work

Research output: Contribution to journalArticle

61 Citations (Scopus)

Abstract

A kindred is described with a dominantly inherited "pure" cerebellar ataxia in which the currently known spinocerebellar ataxias have been excluded. In the eight subjects studied, a notable clinical feature is slow progression, with the three least affected having only a mild degree of gait ataxia after three or more decades of disease duration. Pending an actual chromosomal locus discovery, the name spinocerebellar ataxia (SCA)15 is expectantly applied.

Original languageEnglish
Pages (from-to)1913-1915
Number of pages3
JournalNeurology
Volume57
Issue number10
Publication statusPublished - 27 Nov 2001
Externally publishedYes

Fingerprint Dive into the research topics of 'A new autosomal dominant pure cerebellar ataxia'. Together they form a unique fingerprint.

  • Cite this

    Storey, E., Gardner, R. J. M., Knight, M. A., Kennerson, M. L., Tuck, R. R., Forrest, S. M., & Nicholson, G. A. (2001). A new autosomal dominant pure cerebellar ataxia. Neurology, 57(10), 1913-1915.