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Mov Disord ; 18(8): 914-9, 2003 Aug.
Article in English | MEDLINE | ID: mdl-12889082

ABSTRACT

Autosomal recessive juvenile parkinsonism (AR-JP) is a form of hereditary parkinsonism characterized by variable clinical presentations and caused by mutations in a novel gene, parkin, on chromosome 6q25.2-27. Until now, no Russian cases of parkin-associated AR-JP have been reported on. We recruited 16 patients from 11 Russian families with dopa-responsive movement disorders according to the following criteria: 1) family history compatible with autosomal recessive inheritance; 2) onset of symptoms at A). The majority of our parkin-associated cases were characterized by early-onset dopa-responsive parkinsonism with benign course and slow progression (5 patients from two families have been followed for as long as 18-36 years), and 1 patient had a phenotype of dopa-responsive dystonia. This first description of Russian patients with AR-JP and molecularly proven parkin mutations confirms the widespread occurrence of this polymorphic hereditary extrapyramidal disorder.


Subject(s)
Parkinsonian Disorders/ethnology , Parkinsonian Disorders/genetics , Point Mutation/genetics , Ubiquitin-Protein Ligases/genetics , Adult , Antiparkinson Agents/therapeutic use , DNA Mutational Analysis , GTP Cyclohydrolase/genetics , Humans , Levodopa/therapeutic use , Middle Aged , Parkinsonian Disorders/drug therapy , Pedigree , Severity of Illness Index
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