Autosomal dominant cerebellar ataxia type 1 (Q85240): Difference between revisions
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Ataxia cerebelar autossômica dominante tipo 1 (ACAD) é um grupo das ataxias espinocerebelares (SCA) caracterizadas por ataxia com outros sinais neurológicos, incluindo distúrbios oculomotores, déficits cognitivos, disfunção piramidal e extrapiramidal, comprometimento bulbar, espinal e de sistema nervoso periférico. | |||
| description / en | description / en | ||
Type I autosomal dominant cerebellar ataxia (ADCA) is a group of spinocerebellar ataxias (SCA) characterised by ataxia with other neurological signs, including oculomotor disturbances, cognitive deficits, pyramidal and extrapyramidal dysfunction, bulbar, spinal and peripheral nervous system involvement. | |||
Revision as of 10:36, 15 August 2026
Type I autosomal dominant cerebellar ataxia (ADCA) is a group of spinocerebellar ataxias (SCA) characterised by ataxia with other neurological signs, including oculomotor disturbances, cognitive deficits, pyramidal and extrapyramidal dysfunction, bulbar, spinal and peripheral nervous system involvement.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1919353698 |
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| English | Autosomal dominant cerebellar ataxia type 1 |
Type I autosomal dominant cerebellar ataxia (ADCA) is a group of spinocerebellar ataxias (SCA) characterised by ataxia with other neurological signs, including oculomotor disturbances, cognitive deficits, pyramidal and extrapyramidal dysfunction, bulbar, spinal and peripheral nervous system involvement. |
