Rapid-onset dystonia-parkinsonism (Q98787): Difference between revisions
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Distonia-parkinsonismo de início rápido (DPR) é um transtorno do movimento caracterizado pelo início abrupto de distonia e parkinsonismo em adultos jovens. É devido a uma mutação no gene ATP1A3. É alélica com hemiplegia alternante da infância. | |||
| description / en | description / en | ||
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. | |||
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 |
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| 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. |
