Spinocerebellar ataxia type 26 (Q101086): Difference between revisions
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Ataxia espinocerebelar tipo 26 é um subtipo muito raro de ataxia cerebelar autossômica dominante tipo 3, descrito até o momento em pacientes de uma família americana de descendência norueguesa, e caracterizada por início tardio e ataxia de marcha lentamente progressiva, e problemas no movimento ocular. | |||
| description / en | description / en | ||
Spinocerebellar ataxia type 26 is a very rare subtype of autosomal dominant cerebellar ataxia type 3, described to date in patients from one American family of Norwegian descent, and characterised by late-onset and slowly progressive gait ataxia, and eye movement problems. | |||
Revision as of 17:53, 16 August 2026
Spinocerebellar ataxia type 26 is a very rare subtype of autosomal dominant cerebellar ataxia type 3, described to date in patients from one American family of Norwegian descent, and characterised by late-onset and slowly progressive gait ataxia, and eye movement problems.
| Language | Label | Description | Also known as |
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| default for all languages | ID_586976339 |
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| English | Spinocerebellar ataxia type 26 |
Spinocerebellar ataxia type 26 is a very rare subtype of autosomal dominant cerebellar ataxia type 3, described to date in patients from one American family of Norwegian descent, and characterised by late-onset and slowly progressive gait ataxia, and eye movement problems. |
