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[家族性对疼痛无反应伴躯体感觉不对称:可能的中枢异常]

[Familial indifference to pain with somatosensory asymmetry: possible central anomaly].

作者信息

Bowsher D, Lahuerta J, Peach B, Venn D, Haywar M, Campbell J, Mumford J, Haggett C

机构信息

Pain Research Institute, University Hospital Aintree, Liverpool L7 AL, U.K.

出版信息

Rev Neurol (Paris). 2002 Feb;158(2):195-202.

Abstract

A family of seven siblings is described. The mother and six siblings have been examined, the eldest and youngest of whom suffer from congenital indifference to pain , although both were ticklish, and itched. The functions examined included somatosensory perception thresholds and autonomic functions; perception thresholds were greatly raised in the painfree subjects and to a lesser extent in some other family members, asymmetrically in all cases, being higher in the dominant hand. Painfree Subject 1 also underwent cerebrospinal fluid analysis at age 16, which showed normal B-endorphin levels but undetectable enkephalins. Electrophysiological tests when a child demonstrated notably that most (raised) measured values were lowered by naloxone. Light microscopic sural nerve biopsy performed on painfree Subject 1 in childhood did not suggest any abnormalities other than a thickened nerve sheath. Threshold asymmetry has not been observed in large numbers of subjects without neurological deficits. There were no significant autonomic changes in any tested family member, though there was some asymmetry. It is suggested that the findings may imply a congenital anomaly of the central nervous system which accounts for the somatosensory, biochemical, and electrophysiological abnormalities.

摘要

本文描述了一个有七个兄弟姐妹的家庭。已对母亲和六个兄弟姐妹进行了检查,其中年龄最大和最小的患有先天性痛觉缺失,不过两人都怕痒且会瘙痒。所检查的功能包括躯体感觉阈值和自主神经功能;无痛觉受试者的感觉阈值大幅升高,其他一些家庭成员也有一定程度升高,所有情况下均不对称,优势手的阈值更高。无痛觉受试者1在16岁时还进行了脑脊液分析,结果显示β - 内啡肽水平正常,但脑啡肽检测不到。当一名儿童进行电生理测试时,结果显著表明,大多数(升高的)测量值会被纳洛酮降低。童年时期对无痛觉受试者1进行的光镜腓肠神经活检显示,除了神经鞘增厚外,未发现任何异常。在大量没有神经功能缺损的受试者中未观察到阈值不对称。任何接受测试的家庭成员均未出现明显的自主神经变化,不过存在一些不对称情况。研究表明,这些发现可能意味着中枢神经系统存在先天性异常,这可以解释躯体感觉、生化和电生理方面的异常。

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