| Literature DB >> 11889248 |
P P Pramstaller1, G Künig, K Leenders, M Kann, K Hedrich, P Vieregge, C G Goetz, C Klein.
Abstract
The authors describe a 37-year-old woman with early-onset hemiparkinsonism (HP) and ipsilateral body hemiatrophy (HA). Genetic analysis revealed a missense mutation (Arg275Trp) and a duplication of exon 7 of parkin. The complementary metabolic and receptor pattern of PET ligands corresponded to that typically found in idiopathic PD, although tracer binding asymmetry was lacking. Parkin mutations should be considered in HPHA, particularly when there is a younger age at onset and dystonia is an early sign.Entities:
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Year: 2002 PMID: 11889248 DOI: 10.1212/wnl.58.5.808
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910