Spinocerebellar ataxia type 5 (Q101079): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| Property / Collection date | |||||||||||||||
15 August 2026
| |||||||||||||||
| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 17:52, 16 August 2026
Spinocerebellar ataxia type 5 is a rare subtype of autosomal dominant cerebellar ataxia type 3, characterised by the early-onset of cerebellar signs and eye movement abnormalities with a very slow disease progression (disease duration of more than 30 years). It is due to a mutation in the SPTBN2 gene.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_78905851 |
||
| English | Spinocerebellar ataxia type 5 |
Spinocerebellar ataxia type 5 is a rare subtype of autosomal dominant cerebellar ataxia type 3, characterised by the early-onset of cerebellar signs and eye movement abnormalities with a very slow disease progression (disease duration of more than 30 years). It is due to a mutation in the SPTBN2 gene. |
Statements
CID11:ID_78905851
0 references
dki-india-ID_78905851
0 references
Concluído
0 references
15 August 2026
0 references
