Clinical features and neuroimaging of PARK7-linked parkinsonism

  • M Dekker*
  • , V Bonifati
  • , J van Swieten
  • , R J Galjaard
  • , M Horstink
  • , P Heutink
  • , B Oostra
  • , C van Duijn
  • *Corresponding author for this work

    Research output: Contribution to journalReview articlepeer-review

    78 Citations (Scopus)

    Abstract

    We recently reported linkage to chromosome 1p36 (the PARK7-locus) in a family with early-onset parkinsonism. Linkage to this locus has since been confirmed in an independent data set. We describe clinical and neuroimaging features of the 4 patients in the original PARK7-linked kindred. Age at onset of parkinsonism varied from 27 to 40 years. Clinical progression was slow, and response to dopaminergic therapy good. The clinical spectrum ranged from mild hypokinesia and rigidity, to severe parkinsonism with levodopa-induced dyskinesias and motor fluctuation. Three of four patients with PARK7-linked parkinsonisin exhibited psychiatric disturbances. Structural neuroimaging was unremarkable, but functional imaging of the brain, carried out in 3 patients, showed significant evidence for a presynaptic dopamine deficit, and assessment of cerebral glucose metabolism, as carried out in I patient, showed possible cerebellar involvement. (C) 2003 Movement Disorder Society.

    Original languageEnglish
    Pages (from-to)751-757
    Number of pages7
    JournalMovement Disorders
    Volume18
    Issue number7
    DOIs
    Publication statusPublished - Jul-2003

    Keywords

    • autosomal-recessive parkinsonism
    • PARK7
    • genetics
    • phenotype
    • neuroimaging
    • EARLY-ONSET PARKINSONISM
    • NIGROSTRIATAL DOPAMINERGIC SYSTEM
    • FAMILIAL PARKINSONISM
    • HOMOZYGOUS DELETION
    • DISEASE
    • GENE
    • MUTATIONS
    • LOCUS
    • LOCALIZATION
    • MAPS

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