| Literature DB >> 31779818 |
Alessio Di Fonzo1, Giulia Franco1, Paolo Barone2, Roberto Erro2.
Abstract
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.Entities:
Keywords: ATP1A3; DRD; DYT; Dystonia-parkinsonism; Iron accumulation; NBIA; Neurotransmitter transporters; PRKRA; TAF1; Wilson disease
Mesh:
Year: 2019 PMID: 31779818 DOI: 10.1016/bs.irn.2019.10.007
Source DB: PubMed Journal: Int Rev Neurobiol ISSN: 0074-7742 Impact factor: 3.230