A new autosomal dominant pure cerebellar ataxia.
Neurology
; 57(10): 1913-5, 2001 Nov 27.
Article
in En
| MEDLINE
| ID: mdl-11723290
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.
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Collection:
01-internacional
Database:
MEDLINE
Main subject:
Chromosome Aberrations
/
Spinocerebellar Ataxias
/
Genes, Dominant
Type of study:
Diagnostic_studies
Limits:
Adult
/
Aged
/
Female
/
Humans
/
Male
/
Middle aged
Language:
En
Journal:
Neurology
Year:
2001
Document type:
Article
Affiliation country:
Australia