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家族性自主神经功能异常中睫状神经节和蝶腭神经节的定量研究。

Quantitative studies of ciliary and sphenopalatine ganglia in familial dysautonomia.

作者信息

Pearson J, Pytel B

出版信息

J Neurol Sci. 1978 Nov;39(1):123-30. doi: 10.1016/0022-510x(78)90193-4.

Abstract

In 3 patients with familial dysautonomia (FD) sphenopalatine ganglia were less than one fifth normal in volume and their total neuronal content was reduced to a mean of 1,510 (control mean 56,500). Parasympathetic denervation accounts for absence of overflow tears in FD. Ciliary ganglia were not reduced in volume and in 4 patients the mean neuron total was only slightly diminished to 2,900 (control 3,670, P less than or equal to 0.05). This does not appear sufficient to account for pupillary supersensitivity to methacholine in FD on the basis of denervation. Temporal differences in the embryogenesis of sphenopalatine and ciliary ganglia may underlie the observed differences in neuronal populations and suggest that the developmental anomaly in FD does not occur early in gestation.

摘要

在3例家族性自主神经功能障碍(FD)患者中,蝶腭神经节体积不到正常的五分之一,其神经元总数降至平均1510个(对照组平均为56500个)。副交感神经去神经支配是FD患者无溢泪的原因。睫状神经节体积未减小,4例患者的神经元总数仅略有减少,降至2900个(对照组为3670个,P≤0.05)。基于去神经支配,这似乎不足以解释FD患者对乙酰甲胆碱的瞳孔超敏反应。蝶腭神经节和睫状神经节胚胎发生的时间差异可能是观察到的神经元群体差异的基础,并表明FD的发育异常并非发生在妊娠早期。

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