Autosomal dominant cerebellar ataxia type 4 (Q85247): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Verification Status | |||
Concluído | |||
| Property / Verification Status: Concluído / rank | |||
Normal rank | |||
Revision as of 10:36, 15 August 2026
Autosomal dominant cerebellar movement disorder characterized by ataxia, atrophy, unsteady gait, dysarthria, and distinct peripheral neuropathy. Typically begins in the fourth or fifth decade of life, with continued progression of symptoms. Considered a Type III ADCA that is associated with a mutation at the 16q22 gene locus.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_745970501 |
||
| English | Autosomal dominant cerebellar ataxia type 4 |
Autosomal dominant cerebellar movement disorder characterized by ataxia, atrophy, unsteady gait, dysarthria, and distinct peripheral neuropathy. Typically begins in the fourth or fifth decade of life, with continued progression of symptoms. Considered a Type III ADCA that is associated with a mutation at the 16q22 gene locus. |
Statements
CID11:ID_745970501
0 references
dki-india-ID_745970501
0 references
Concluído
0 references
