| Literature DB >> 16267847 |
Angelo Antonini1, Stefano Goldwurm, Riccardo Benti, Holger Prokisch, Monika Ebhardt, Roberto Cilia, Michela Zini, Andrea Righini, Giovanni Cossu, Gianni Pezzoli.
Abstract
We report on a patient with late-onset, pantothenate kinase-associated neurodegeneration (PKAN) who revealed two new heterozygous mutations at gene testing and showed asymmetric moderately reduced striatal dopamine transporter binding with single photon emission computed tomography, possibly due to prolonged neuroleptic treatment. These findings expand the genetic and imaging spectrum of this rare disorder. (c) 2005 Movement Disorder Society.Entities:
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Year: 2006 PMID: 16267847 DOI: 10.1002/mds.20774
Source DB: PubMed Journal: Mov Disord ISSN: 0885-3185 Impact factor: 10.338