Rapid-onset dystonia-parkinsonism (Q98787): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| (One intermediate revision by the same user not shown) | |||||||||||||||
| 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 15:23, 16 August 2026
Rapid-onset dystonia-parkinsonism (RDP) is a movement disorder characterised by abrupt onset of dystonia and parkinsonism in young adults. It is due to a mutation in the ATP1A3 gene. It is allelic with alternating hemiplegia of childhood.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_878904788 |
||
| English | Rapid-onset dystonia-parkinsonism |
Rapid-onset dystonia-parkinsonism (RDP) is a movement disorder characterised by abrupt onset of dystonia and parkinsonism in young adults. It is due to a mutation in the ATP1A3 gene. It is allelic with alternating hemiplegia of childhood. |
Statements
CID11:ID_878904788
0 references
dki-india-ID_878904788
0 references
Concluído
0 references
15 August 2026
0 references
