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

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 journal › Article › peer-review

72 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 language	English
Pages (from-to)	1913-1915
Number of pages	3
Journal	Neurology
Volume	57
Issue number	10
Publication status	Published - 27 Nov 2001
Externally published	Yes

Cite this

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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.",

author = "E. Storey and Gardner, {R. J.M.} and Knight, {M. A.} and Kennerson, {M. L.} and Tuck, {R. R.} and Forrest, {S. M.} and Nicholson, {G. A.}",

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T1 - A new autosomal dominant pure cerebellar ataxia

AU - Storey, E.

AU - Gardner, R. J.M.

AU - Knight, M. A.

AU - Kennerson, M. L.

AU - Tuck, R. R.

AU - Forrest, S. M.

AU - Nicholson, G. A.

PY - 2001/11/27

Y1 - 2001/11/27

N2 - 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.

AB - 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.

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M3 - Article

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AN - SCOPUS:0035960565

SN - 0028-3878

VL - 57

SP - 1913

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JO - Neurology

JF - Neurology

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ER -

A new autosomal dominant pure cerebellar ataxia

Abstract

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