ATP1A3 mutations in infants: a new rapid-onset dystonia-Parkinsonism phenotype characterized by motor delay and ataxia

We report new clinical features of delayed motor development, hypotonia, and ataxia in two young children with mutations (R756H and D923N) in the ATP1A3 gene. In adults, mutations in ATP1A3 cause rapid-onset dystonia-Parkinsonism (RDP, DYT12) with abrupt onset of fixed dystonia. The parents and chil...

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Bibliographic Details
Main Authors:	BRASHEAR, ALLISON, MINK, JONATHAN, HILL, DEBORAH F, BOGGS, NIKI, MCCALL, W VAUGHN, STACY, MARK, SNIVELY, BEVERLY, LIGHT, L S, SWEADNER, KATHLEEN, OZELIUS, LAURIE J, MORRISON, LESLIE
Format:	Artigo
Language:	Inglês
Published:	2012
Subjects:	Article
Online Access:	https://ncbi.nlm.nih.gov/pmc/articles/PMC3465467/ https://ncbi.nlm.nih.gov/pubmed/22924536 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1469-8749.2012.04421.x
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ATP1A3 mutations in infants: a new rapid-onset dystonia-Parkinsonism phenotype characterized by motor delay and ataxia

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