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Dystonia 12

MONDO:0007496

Rapid-onset dystonia-parkinsonism (RDP) is a very rare movement disorder, characterized by the abrupt onset of parkinsonism and dystonia, often triggered by physical or psychological stress.

Also known as: ATP1A3 dystonic disorder, DYT-ATP1A3, DYT12, dystonia 12, dystonia type 12, dystonia-12, dystonic disorder caused by mutation in ATP1A3, RDP

28 clinical trials for this condition and its sub-types, 2 tagged with Dystonia 12 itself.

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Where it sits in the disease tree

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Part of

↑ Parkinsonian disorder (1315) ↑ Combined dystonia (12) ↑ ATP1A3-associated neurological disorder (2)

Including sub-types (28) Tagged with Dystonia 12 (2)

Trials to join now! 1 Not yet finished but already full! 1

Scientists track rare dystonia to map its genetic roots

Knowledge-focused Ongoing

This study is observing up to 198 people with rapid-onset dystonia-parkinsonism (RDP) or related genetic mutations. Researchers aim to identify affected individuals, document how common the disease is, and track its progression over time. Participants undergo assessments of sympt…

Sponsor: State University of New York at Buffalo • Aim: Knowledge-focused

Last updated Jun 27, 2026 12:29 UTC

Dystonia 12

Where it sits in the disease tree

Scientists track rare dystonia to map its genetic roots