期刊
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY
卷 15, 期 3, 页码 271-275出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.ejpn.2011.01.001
关键词
Juvenile parkinsonism; ATP13A2 gene; Heterozygous mutation; [(123)I] SPECT; PARK9
We report a case of levodopa-responsive juvenile parkinsonism (JP) associated with a heterozygous ATP13A2 gene frameshift mutation. The clinical phenotype of our case is more severe when compared with other published reports of symptomatic heterozygous ATP13A2 mutation carriers. To our knowledge, this is the youngest reported patient with JP associated with a heterozygous ATP13A2 mutation. Our findings expand the clinical phenotypic spectrum of JP associated with heterozygous ATP13A2 mutation. (C) 2011 European Paediatric Neurology Society. Published by Elsevier Ltd. All rights reserved.
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