Bruno Michiko K, Ravina Bernard, Garraux Gaetan, Hallett Mark, Ptacek Louis, Singleton Amanda, Johnson Janel, Singleton Andrew, Hanson Melissa, Considine Elaine, Gwinn-Hardy Katrina
Parkinson's Unit, Division of Neurogenetics, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA.
Mov Disord. 2004 Feb;19(2):228-30. doi: 10.1002/mds.10626.
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.
阵发性运动诱发性肌张力障碍可与帕金森病(PD)同时出现,在极少数情况下,这也可能是首发症状。我们报告了2名二级表亲(无已知血缘关系),他们表现为阵发性运动诱发性肌张力障碍,后来出现了PD的临床特征。尽管提示为常染色体隐性遗传,且肌张力障碍特征进一步提示帕金蛋白可能是病因,但帕金蛋白突变测序结果为阴性,这个家族可能代表了PD的一种遗传变异型。对这个家族及类似家族进行进一步的基因型-表型研究,可能会为PD的症状前表现提供线索,并可能反映出未来遗传学研究感兴趣的一种特殊表型。