Huntington-Krankheit und Chorea minor
Research output: Contribution to journal › Research article › Invited › peer-review
Contributors
Abstract
Huntington's disease was an important example for discussing the problem of predictive genetic testing. Like other movement disorders, it includes non-motor symptoms and a prodromal phase. As a rapidly progressive monogenetic disease, it is an important model disease for the study of neurodegenerative pathomechanisms and one of the first movement disorders for which causal therapies seem to be reachable.
Translated title of the contribution | Huntington's disease and Sydenham's chorea |
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Details
Original language | German |
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Pages (from-to) | 403-415 |
Number of pages | 13 |
Journal | Fortschritte der Neurologie, Psychiatrie : FDN |
Volume | 88 |
Issue number | 6 |
Publication status | Published - Jun 2020 |
Peer-reviewed | Yes |
External IDs
Scopus | 85086721968 |
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ORCID | /0000-0002-2387-526X/work/150328972 |
Keywords
Keywords
- Genetic Testing, Humans, Huntington Disease/diagnosis, Prodromal Symptoms