Facheris Maurizio Francesco, Maniak Susanna, Scaravilli Francesco, Schüle Birgit, Klein Christine, Pramstaller Peter Paul
Department of Neurology, Central Hospital Bolzano-Bozen, Bolzano-Bozen, Italy.
Parkinsonism Relat Disord. 2008 Aug;14(6):517-9. doi: 10.1016/j.parkreldis.2007.11.004. Epub 2008 Mar 5.
Pure akinesia (PA) is a rare neurodegenerative condition that may represent a limited expression of progressive supranuclear palsy (PSP). Only a few pathological studies have been reported and its classification remains unclear. We report the case of a 57-year-old Caucasian man who was initially clinically diagnosed with classical PA. After four years the patient developed additional symptoms and signs compatible with the diagnosis of clinically probable PSP. The diagnosis of PSP was confirmed by post-mortem examination. Genetic analysis of the MAPT gene revealed an A0/A0 genotype, which has been repeatedly associated with the PSP phenotype, and might discriminate between PA and other gait disorders. Our case strengthens the hypothesis that PA should be considered as initial manifestation of PSP.
纯运动不能(PA)是一种罕见的神经退行性疾病,可能是进行性核上性麻痹(PSP)的一种有限表现形式。仅报道过少数病理研究,其分类仍不明确。我们报告一例57岁白种男性病例,该患者最初临床诊断为典型PA。四年后,患者出现了与临床很可能为PSP诊断相符的其他症状和体征。PSP诊断经尸检证实。对微管相关蛋白tau(MAPT)基因的遗传分析显示为A0/A0基因型,该基因型反复与PSP表型相关,且可能有助于区分PA与其他步态障碍。我们的病例强化了PA应被视为PSP初始表现的假说。