Spinocerebellar ataxia type 12 (Q101082): Difference between revisions
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Ataxia espinocerebelar tipo 12 (SCA12) é um subtipo muito raro de ataxia cerebeçar autossômica dominante tipo 1 (ACAD tipo I). É caracterizada pela presença de tremor de ação associado a ataxia cerebelar relativamente leve. Sinais piramidais e extra-piramidais associados e demência têm sido reportados. | |||
| description / en | description / en | ||
Spinocerebellar ataxia type 12 (SCA12) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterised by the presence of action tremor associated with relatively mild cerebellar ataxia. Associated pyramidal and extrapyramidal signs and dementia have been reported. | |||
Revision as of 17:52, 16 August 2026
Spinocerebellar ataxia type 12 (SCA12) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterised by the presence of action tremor associated with relatively mild cerebellar ataxia. Associated pyramidal and extrapyramidal signs and dementia have been reported.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1210063722 |
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| English | Spinocerebellar ataxia type 12 |
Spinocerebellar ataxia type 12 (SCA12) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterised by the presence of action tremor associated with relatively mild cerebellar ataxia. Associated pyramidal and extrapyramidal signs and dementia have been reported. |
