Abstract
Paroxysmal exercise-induced dystonia can occur with Parkinson's disease (PD), and in rare cases, this can also be the presenting symptom. We report on 2 second cousins (no known consanguinity) who presented with paroxysmal exercise-induced dystonia who later developed clinical features of PD. Although autosomal recessive inheritance was suggested, and the dystonic features further suggest parkin as a possible cause, sequencing for parkin mutations was negative and this family may represent a genetic variant of PD. Further genotype-phenotype studies in this and similar families may give clues to pre-symptomatic symptoms in PD and may reflect a particular phenotype of interest for genetics studies in the future.
Publication types
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Case Reports
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Aged
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Antiparkinson Agents / therapeutic use
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Carbidopa / therapeutic use
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DNA Mutational Analysis
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Disease Progression
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Drug Combinations
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Dystonic Disorders / diagnosis
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Dystonic Disorders / drug therapy
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Dystonic Disorders / genetics*
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Exercise*
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Female
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Genotype
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Humans
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Levodopa / therapeutic use
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Male
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Middle Aged
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Neurologic Examination / drug effects
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Parkinsonian Disorders / diagnosis
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Parkinsonian Disorders / genetics*
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Phenotype
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Semen
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Ubiquitin-Protein Ligases / genetics
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Videotape Recording
Substances
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Antiparkinson Agents
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Drug Combinations
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carbidopa, levodopa drug combination
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Levodopa
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Ubiquitin-Protein Ligases
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parkin protein
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Carbidopa