Spinocerebellar ataxia type 26 (Q101086): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed label, description and/or aliases in pt-br, en |
Changed an Item |
||
| Property / Canonical URI | |||
| Property / Canonical URI: https://id.who.int/icd/entity/586976339 / rank | |||
Normal rank | |||
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 |
|---|---|---|---|
| default for all languages | ID_586976339 |
||
| 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. |
