Huntington-Krankheit und Chorea minor

Publikation: Beitrag in FachzeitschriftForschungsartikelEingeladenBegutachtung

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.

Details

OriginalspracheDeutsch
Seiten (von - bis)403-415
Seitenumfang13
FachzeitschriftFortschritte der Neurologie, Psychiatrie : FDN
Jahrgang88
Ausgabenummer6
PublikationsstatusVeröffentlicht - Juni 2020
Peer-Review-StatusJa

Externe IDs

Scopus 85086721968
ORCID /0000-0002-2387-526X/work/150328972

Schlagworte

Schlagwörter

  • Genetic Testing, Humans, Huntington Disease/diagnosis, Prodromal Symptoms