A case of rapid-onset dystonia-parkinsonism accompanied by pyramidal tract impairment

BACKGROUND: Rapid-onset dystonia-parkinsonism (RDP) is a rare autosomal dominant disorder that is caused by mutations in the ATP1A3 gene and is characterized by an acute onset of asymmetric dystonia and parkinsonism. To date, fewer than 75 RDP cases have been reported worldwide. Clinical signs of py...

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Detalles Bibliográficos
Autores principales: Liu, Yanqiu, Lu, Yan, Zhang, Xinqing, Xie, Shuping, Wang, Tingting, Wu, Tianwen, Wang, Chaoyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5105251/
https://www.ncbi.nlm.nih.gov/pubmed/27835968
http://dx.doi.org/10.1186/s12883-016-0743-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5105251/
https://www.ncbi.nlm.nih.gov/pubmed/27835968
http://dx.doi.org/10.1186/s12883-016-0743-8

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