Spinocerebellar ataxia type 6 (Q101078): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| (2 intermediate revisions by the same user not shown) | |||||||||||||||
| Property / Verification Status | |||||||||||||||
Concluído | |||||||||||||||
| Property / Verification Status: Concluído / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Knowledge Architect | |||||||||||||||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
Normal rank | |||||||||||||||
| 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 6 is a common subtype of autosomal dominant cerebellar ataxia type 3, most commonly seen in Japan, Korea, the Netherlands and Germany, characterised by late-onset and slowly progressive gait ataxia, cerebellar signs and eye movement problems and caused by mutations in the CACNA1A gene.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1056119281 |
||
| English | Spinocerebellar ataxia type 6 |
Spinocerebellar ataxia type 6 is a common subtype of autosomal dominant cerebellar ataxia type 3, most commonly seen in Japan, Korea, the Netherlands and Germany, characterised by late-onset and slowly progressive gait ataxia, cerebellar signs and eye movement problems and caused by mutations in the CACNA1A gene. |
Statements
CID11:ID_1056119281
0 references
dki-india-ID_1056119281
0 references
Concluído
0 references
15 August 2026
0 references
