Adult-onset dystonia-parkinsonism
What is Adult-onset dystonia-parkinsonism?
A rare neurodegenerative disease usually presenting before the age of 30 and which is characterized by dystonia, L-dopa-responsive parkinsonism, pyramidal signs and rapid cognitive decline.
Other condition names
- Dystonia-parkinsonism, Paisan-Ruiz type
- PARK14
- PLA2G6-related dystonia-parkinsonism
Inheritance type
Autosomal recessive
Prevalence
- Worldwide: <1 in 1,000 000
Age of Onset
- Adolescent
- Adult
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on "https://www.orphadata.com". Data version 1.3.16 / 4.1.7.