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唐氏综合征患儿的树突萎缩

Dendritic atrophy in children with Down's syndrome.

作者信息

Becker L E, Armstrong D L, Chan F

出版信息

Ann Neurol. 1986 Oct;20(4):520-6. doi: 10.1002/ana.410200413.

Abstract

Dendritic branching was evaluated in the visual cortex of 8 children with Down's syndrome and 10 controls, ranging in age from 4 months to 7 years and divided into infantile, late-infantile, and juvenile groups. Camera lucida drawings of Golgi-impregnated neurons were used for examining the following dendritic aspects: dendritic intersections as a function of distance from the cell body, point of maximum dendritic branching, number of branch orders, total number of branch segments, and total dendritic length. The number of intersections and the total dendritic length were above normal in the infantile period (6 months old or less) and dropped steadily to significantly below normal in the juvenile group (older than 2 years). These reductions contrasted with expanding dendritic arborization in normal children. The results suggest that the dendritic tree atrophies in early childhood in Down's syndrome.

摘要

对8名唐氏综合征患儿和10名对照儿童的视觉皮层进行了树突分支评估,这些儿童年龄在4个月至7岁之间,分为婴儿期、晚婴儿期和青少年期组。使用高尔基染色神经元的明视野绘图来检查以下树突方面:作为距细胞体距离函数的树突交叉点、最大树突分支点、分支级数、分支段总数和总树突长度。交叉点数量和总树突长度在婴儿期(6个月及以下)高于正常水平,并在青少年组(2岁以上)稳步下降至显著低于正常水平。这些减少与正常儿童不断扩展的树突分支形成对比。结果表明,唐氏综合征患儿在幼儿期树突会萎缩。

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