Dystonia due to dentatorubropallidoluysian atrophy (Q98789): Difference between revisions
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Distonia devido à atrofia dentato-rubro-pálido-luisiana (DRPLA), um subtipo raro de ataxia cerebelar autossômica dominante tipo I (ADCA tipo I). DRPLA é caracterizada por movimentos involuntários, ataxia, epilepsia, transtornos mentais, declínio cognitivo e antecipação marcante. | |||
| description / en | description / en | ||
Dystonia due to dentatorubral pallidoluysian atrophy (DRPLA), a rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). DRPLA is characterised by involuntary movements, ataxia, epilepsy, mental disorders, cognitive decline and prominent anticipation. | |||
Revision as of 15:23, 16 August 2026
Dystonia due to dentatorubral pallidoluysian atrophy (DRPLA), a rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). DRPLA is characterised by involuntary movements, ataxia, epilepsy, mental disorders, cognitive decline and prominent anticipation.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_960247356 |
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| English | Dystonia due to dentatorubropallidoluysian atrophy |
Dystonia due to dentatorubral pallidoluysian atrophy (DRPLA), a rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). DRPLA is characterised by involuntary movements, ataxia, epilepsy, mental disorders, cognitive decline and prominent anticipation. |
