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首页> 外文期刊>European journal of neurology: the official journal of the European Federation of Neurological Societies >Clinical characteristics of the alpha-synuclein mutation (G209A)-associated Parkinson's disease in comparison with other forms of familial Parkinson's disease in Greece.
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Clinical characteristics of the alpha-synuclein mutation (G209A)-associated Parkinson's disease in comparison with other forms of familial Parkinson's disease in Greece.

机译:与希腊其他形式的家族性帕金森氏病相比,α-突触核蛋白突变(G209A)相关的帕金森氏病的临床特征。

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An Ala53Thr mutation of the alpha-synuclein has been recently identified as a rare cause of familial Parkinson's disease (fPD). In the present study, the clinical characteristics of Parkinson's disease (PD) patients with Ala53Thr alpha-synuclein mutation (alpha-synPD) were compared with fPD patients without any known mutation. An investigator blinded to the results of the genetic analysis examined 15 alpha-synPD patients and 43 consecutive fPD patients. Demographic data, age at onset of the illness, duration of the disease and modality of presentation were collected. Segregation ratios for both sexes in individuals at risk of developing alpha-synPD were estimated. The Unified Parkinson's disease rating scale (UPDRS) was also completed. The 15 alpha-synPD patients were matched for duration of the disease and age at onset with 15 of the 43 fPD patients (MfPD). Comparisons were also made between 14 patients belonging to three multicase families with patterns of inheritance similar to alpha-synPD. The alpha-synPD patients were significantly younger (mean difference 11.8 years) and showed the first sign of the disease earlier in life (mean difference 12.7 years) as compared with the fPD patients. Tremor at onset was present in only one (6.7%) of the alpha -synPD patients compared with 18 (41.9%) of the fPD patients (P = 0.01). At the time of examination rigidity, postural instability, orthostatic hypotension and the overall clinical severity did not differ significantly either between alpha-synPD and fPD or between alpha-synPD and MfPD groups. Nevertheless, some clinically relevant trends concerning the psychiatric symptoms and complications of therapy were recognized. The overall clinical severity and the progression of the disease in patients with alpha-synPD did not differ from that of the fPD patients. The alpha-synPD patients presented the illness at a younger age and also had lower prevalence of tremor when compared with the fPD patients.
机译:最近发现,α-突触核蛋白的Ala53Thr突变是家族性帕金森氏病(fPD)的罕见原因。在本研究中,将具有Ala53Thrα-突触核蛋白突变(alpha-synPD)的帕金森氏病(PD)患者与没有任何已知突变的fPD患者的临床特征进行了比较。一位研究人员对遗传分析的结果视而不见,对15位α-synPD患者和43位连续的fPD患者进行了检查。收集人口统计数据,发病年龄,疾病持续时间和表现方式。估计有患​​α-synPD危险的个体中男女的隔离率。帕金森病综合评分表(UPDRS)也已完成。 15名α-synPD患者的疾病持续时间和发病年龄与43名fPD患者中的15名(MfPD)相匹配。还比较了14个属于三个多病例家族的患者的遗传模式,这些遗传模式类似于alpha-synPD。与fPD患者相比,α-synPD患者明显年轻(平均差异11.8岁),并且在生命早期显示出该疾病的首发征兆(平均差异12.7岁)。只有1名(6.7%)α-synPD患者出现震颤,而18名fPD患者(41.9%)出现震颤(P = 0.01)。在检查刚度时,α-synPD和fPD之间或α-synPD和MfPD组之间的姿势不稳,体位性低血压和整体临床严重性无明显差异。然而,人们认识到一些有关精神症状和治疗并发症的临床相关趋势。 α-synPD患者的总体临床严重程度和疾病进展与fPD患者没有差异。与fPD患者相比,α-synPD患者在年轻时发病,震颤发生率也较低。

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