| Literature DB >> 17149727 |
Maria Teresa Pellecchia1, Andrea Varrone, Grazia Annesi, Marianna Amboni, Giulio Cicarelli, Valeria Sansone, Ferdinanda Annesi, Francesca Emanuela Rocca, Carmine Vitale, Sabina Pappatà, Aldo Quattrone, Paolo Barone.
Abstract
We report a family with 5 affected individuals manifesting either essential tremor (ET), Parkinsonism, or both, consistent with pseudo-dominant inheritance of PARK2. Two homozygotes presented postural and kinetic tremor several years before the onset of Parkinsonism. Postural and kinetic tremor mimicking ET was the only feature in 1 homozygous and 2 heterozygous carriers of the mutation. Striatal dopamine transporter density was reduced in accordance with phenotype and number of mutated alleles. In 3 homozygotes and 1 heterozygote, a 2-year follow-up single photon emission computed tomography suggested no progression of nigrostriatal deficit. (c) 2006 Movement Disorder Society.Entities:
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Year: 2007 PMID: 17149727 DOI: 10.1002/mds.21262
Source DB: PubMed Journal: Mov Disord ISSN: 0885-3185 Impact factor: 10.338