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非先天性强直性肌营养不良患者的智力功能和人格

Intellectual functions and personality in subjects with noncongenital myotonic muscular dystrophy.

作者信息

Franzese A, Antonini G, Iannelli M, Leardi M G, Spada S, Vichi R, Millefiorini M, Lazzari R

机构信息

Institute of Psychology, Medical School, Rome, Italy.

出版信息

Psychol Rep. 1991 Jun;68(3 Pt 1):723-32. doi: 10.2466/pr0.1991.68.3.723.

Abstract

Mental retardation and personality disorders are commonly described among the symptoms of myotonic dystrophy. Nevertheless, this tendency is not supported by systematic studies performed on large samples, whose results are controversial. We studied the cognitive functions and personalities of a group of 28 patients, in whom myotonic dystrophy had commenced in juvenile or adult life. The severity of the disease was variable, but all subjects were self-sufficient. Only 7.1% of subjects showed low intelligence with deterioration of perceptual-motor functions. This was not correlated with the severity of their disease. Women had a substantially lower mean Wechsler-Bellevue score than men. The personality function study of the entire group showed no change of psychiatric relevance but did present a depressive attitude with marked somatic concern and difficulties in establishing relationships in social life.

摘要

智力迟钝和人格障碍在强直性肌营养不良的症状中很常见。然而,这种趋势并未得到对大量样本进行的系统研究的支持,其结果存在争议。我们研究了一组28名患者的认知功能和人格,这些患者的强直性肌营养不良始于青少年期或成年期。疾病的严重程度各不相同,但所有受试者都能自理。只有7.1%的受试者表现出智力低下且感知运动功能退化。这与他们疾病的严重程度无关。女性的韦克斯勒-贝尔维尤平均得分显著低于男性。对整个组的人格功能研究表明,没有与精神相关的变化,但确实表现出一种抑郁态度,伴有明显的躯体关注以及在社会生活中建立人际关系存在困难。

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