Parkinsonism in diseases predominantly presenting with dystonia.
ATP1A3
DRD
DYT
Dystonia-parkinsonism
Iron accumulation
NBIA
Neurotransmitter transporters
PRKRA
TAF1
Wilson disease
Journal
International review of neurobiology
ISSN: 2162-5514
Titre abrégé: Int Rev Neurobiol
Pays: United States
ID NLM: 0374740
Informations de publication
Date de publication:
2019
2019
Historique:
entrez:
30
11
2019
pubmed:
30
11
2019
medline:
2
6
2020
Statut:
ppublish
Résumé
If the presence of dystonia is a well-recognized phenomenon in disorders predominantly presenting with parkinsonism, including sporadic Parkinson Disease, the term dystonia-parkinsonism usually refers to rare conditions, often genetic, in which the severity of dystonia usually equates that of parkinsonism. At variance with parkinsonian syndromes with additional dystonia, the conditions reviewed in this chapter have usually their onset in childhood and their diagnostic work-up is different. In fact, the phenotype is not usually specific of the underlying defect and additional investigations are therefore required. Here, we review the diseases predominantly presenting with dystonia where parkinsonism can develop, according to their main pathophysiological mechanism including disorders of dopamine biosynthesis, neurotransmitter transporter disorders, disorder of metal metabolism (i.e., iron, copper and manganese) and other inherited dystonia-parkinsonism conditions.
Identifiants
pubmed: 31779818
pii: S0074-7742(19)30093-5
doi: 10.1016/bs.irn.2019.10.007
pii:
doi:
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
307-326Informations de copyright
Copyright © 2019 Elsevier Inc. All rights reserved.