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瑞特综合征的解剖学

Anatomy of Rett syndrome.

作者信息

Nomura Y, Segawa M

出版信息

Am J Med Genet Suppl. 1986;1:289-303. doi: 10.1002/ajmg.1320250529.

Abstract

Rett syndrome is a clinical entity with a distinct set of signs and symptoms. Its etiology is unknown. We review here our observations in this disorder based upon clinical and polysomnographic examinations which are consistent with a developmental disorder of the monoaminergic neural system. These studies argue for a disorder of the noradrenergic, serotonergic and dopaminergic system arising in the locus ceruleus, raphe nuclei and substantia nigra, respectively. Because events of rapid eye movement sleep appear not disturbed, except for body movements, cholinergic neurons are probably not affected. Disordered physiologic states appear in a characteristic sequence with advancing age. Clinical symptoms associated with the aberrant caudally located neurons appear early and those rostrally located become manifested later. This caudalorostral developmental process attributable to early lesion of monoaminergic neurons may explain the age-related sequence of symptoms of Rett syndrome.

摘要

瑞特综合征是一种具有独特体征和症状的临床病症。其病因不明。在此,我们基于临床和多导睡眠图检查回顾我们对该病症的观察结果,这些检查结果与单胺能神经系统的发育障碍相符。这些研究表明,分别在蓝斑、中缝核和黑质中出现的去甲肾上腺素能、5-羟色胺能和多巴胺能系统存在紊乱。由于除身体运动外,快速眼动睡眠事件似乎未受干扰,胆碱能神经元可能未受影响。随着年龄增长,紊乱的生理状态会以特征性顺序出现。与位于尾部的异常神经元相关的临床症状出现较早,而位于头部的那些症状则稍后显现。这种归因于单胺能神经元早期损伤的从尾端到头端的发育过程,可能解释了瑞特综合征症状随年龄变化的顺序。

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