Spinocerebellar ataxia type 19 (Q101073): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / CURIE | |||
CID11:ID_1792112140 | |||
| Property / CURIE: CID11:ID_1792112140 / rank | |||
Normal rank | |||
Revision as of 17:52, 16 August 2026
Spinocerebellar ataxia 19 (SCA 19) is a rare subtype of type I autosomal dominant cerebellar ataxia involving a locus on chromosome 1p21-q21. Characterized by mild ataxia, hyporeflexia, myoclonus, postural tremor, cognitive impairment, and frontal lobe dysfunction.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1792112140 |
||
| English | Spinocerebellar ataxia type 19 |
Spinocerebellar ataxia 19 (SCA 19) is a rare subtype of type I autosomal dominant cerebellar ataxia involving a locus on chromosome 1p21-q21. Characterized by mild ataxia, hyporeflexia, myoclonus, postural tremor, cognitive impairment, and frontal lobe dysfunction. |
Statements
CID11:ID_1792112140
0 references
