Golodets R G, Kazakova P B
Zh Nevropatol Psikhiatr Im S S Korsakova. 1983;83(7):1045-53.
Fifteen patients with oligophrenia (6 men and 9 women) who died at the age of 21 to 65 years were studied clinically and morphologically. Two groups were identified: 1) oligophrenia complicated by the convulsive syndrome (8 observations) and 2) oligophrenia without the above syndrome (7 observations). The first group was characterized by gross morphological signs of cerebral dysontogenic disorders and by more pronounced mental retardation. In the second group, cerebral dysontogenic disorders were expressed to a lesser degree; in some cases only at a microscopic level. Despite the differences in the nature and severity of clinical and morphological manifestations of this disease, prenatal impairment of brain development seemed to be a linking element in all the cases under study. The morphological characteristics obtained are suggestive of the exogenic nature of the oligophrenic forms studied.
对15例智力发育迟缓患者(6例男性,9例女性)进行了临床和形态学研究,这些患者年龄在21至65岁之间。确定了两组:1)合并惊厥综合征的智力发育迟缓(8例观察)和2)无上述综合征的智力发育迟缓(7例观察)。第一组的特征是脑发育异常的明显形态学体征和更明显的智力迟钝。在第二组中,脑发育异常的程度较轻;在某些情况下仅在显微镜水平可见。尽管该疾病的临床和形态学表现的性质和严重程度存在差异,但脑发育的产前损伤似乎是所有研究病例中的一个关联因素。所获得的形态学特征提示所研究的智力发育迟缓形式具有外源性。